A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676472



Internal ID15413124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172539573..172540341hg38UCSC Ensembl
Innerchr3:172257363..172258131hg19UCSC Ensembl
Innerchr3:173740057..173740825hg18UCSC Ensembl
Innerchr3:173740065..173740833hg17UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
hg17769
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520204
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676472
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