A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662354



Internal ID15399006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:131318415..131327953hg38UCSC Ensembl
Innerchr12:131802960..131812498hg19UCSC Ensembl
Innerchr12:130368913..130378451hg18UCSC Ensembl
Innerchr12:130327840..130337378hg17UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg389539
hg199539
hg189539
hg179539
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517271
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662354
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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