A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643033



Internal ID18941314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13054314..13091121hg38UCSC Ensembl
Innerchr7:13093939..13130746hg19UCSC Ensembl
Innerchr7:13060464..13097271hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836808
hg1936808
hg1836808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026551
Supporting Variants
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)nssv3643033
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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