A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981607



Internal ID16275563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176088947..176177948hg38UCSC Ensembl
Innerchr3:175806735..175895736hg19UCSC Ensembl
Innerchr3:177289429..177378430hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3889002
hg1989002
hg1889002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592603
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer