A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039792



Internal ID19129011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73538592..73698607hg38UCSC Ensembl
Innerchr12:73932372..74092387hg19UCSC Ensembl
Innerchr12:72218639..72378654hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38160016
hg19160016
hg18160016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3524625
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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