A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026624



Internal ID19115842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12924282..13083783hg38UCSC Ensembl
Innerchr7:12963907..13123408hg19UCSC Ensembl
Innerchr7:12930432..13089933hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38159502
hg19159502
hg18159502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642989
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)nsv1026624
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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