A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697374



Internal ID15434026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110436325..110722318hg38UCSC Ensembl
Innerchr3:110155172..110441165hg19UCSC Ensembl
Innerchr3:111637862..111923855hg18UCSC Ensembl
Innerchr3:111637862..111923855hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38285994
hg19285994
hg18285994
hg17285994
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520365
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697374
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