A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674986



Internal ID15411638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139900227..139902682hg38UCSC Ensembl
Innerchr3:139619069..139621524hg19UCSC Ensembl
Innerchr3:141101759..141104214hg18UCSC Ensembl
Innerchr3:141101767..141104222hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382456
hg192456
hg182456
hg172456
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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