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nsv5444290

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 15 studies. See in: genome view    
Submitted genomic170,763,052-170,763,114Question Mark
Overlapping variant regions from other studies: 111 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):171,619,562-171,619,624Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5444290Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2170,763,052170,763,114
nsv5444290RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2171,619,562171,619,624

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922221duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922221Submitted genomicNC_000002.12:g.170
763052_170763114du
p
GRCh38 (hg38)NC_000002.12Chr2170,763,052170,763,114
nssv16922221RemappedPerfectNC_000002.11:g.171
619562_171619624du
p
GRCh37.p13First PassNC_000002.11Chr2171,619,562171,619,624

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16922221<0.00146398
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