Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4436396

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:complex substitution
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:7,418,850

Description:GRCh37/hg19 15q14-15.1 chr15:34638237..42057083 complex variant AND Spindle cell sarcoma

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 19990 SVs from 133 studies. See in: genome view

Remapped(Score: Perfect):34,346,036-41,764,885

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4436396	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	34,346,036	34,346,036	41,764,885	41,764,885
nsv4436396	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	34,638,237	34,640,169	42,054,561	42,057,083

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754780	complex substitution	Multiple	Multiple	Spindle cell sarcoma	Pathogenic	ClinVar	RCV000714282.1, VCV000585332.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15754780	Remapped	Perfect	GRCh38.p12	First Pass	NC_000015.10	Chr15	34,346,036	34,346,036	41,764,885	41,764,885
nssv15754780	Submitted genomic		GRCh37 (hg19)		NC_000015.9	Chr15	34,638,237	34,640,169	42,054,561	42,057,083

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754780	complex substitution	somatic	Spindle cell sarcoma	Pathogenic	ClinVar	RCV000714282.1, VCV000585332.1

No genotype data were submitted for this variant

You are here: NCBI