A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026551



Internal ID19115769
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 StatusM
Merged Variantsdgv6277n100
Supporting Variantsnssv3643033, nssv3643032
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)nsv1026551
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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