A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668949



Internal ID15058915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:169210..186380hg38UCSC Ensembl
Innerchr12:278376..295546hg19UCSC Ensembl
Innerchr12:148637..165807hg18UCSC Ensembl
Innerchr12:148637..165807hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3817171
hg1917171
hg1817171
hg1717171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515938
Supporting Variants
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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