A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703436



Internal ID15093402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32858582..32863803hg38UCSC Ensembl
Innerchr2:33083649..33088870hg19UCSC Ensembl
Innerchr2:32937153..32942374hg18UCSC Ensembl
Innerchr2:32995300..33000521hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg385222
hg195222
hg185222
hg175222
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516173
Supporting Variants
Samples
Known GenesLINC00486
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703436
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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