A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026321



Internal ID19115538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7285169..7389929hg38UCSC Ensembl
Innerchr7:7324800..7429560hg19UCSC Ensembl
Innerchr7:7291325..7396085hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38104761
hg19104761
hg18104761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6251n100
Supporting Variantsnssv3655093
Samples
Known GenesCOL28A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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