A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156554



Internal ID15853886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101484174hg38UCSC Ensembl
Innerchr7:100968363..101127455hg19UCSC Ensembl
Innerchr7:100755083..100914175hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38159093
hg19159093
hg18159093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607980
Supporting Variants
Samples1780854477_A
Known GenesCOL26A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156554
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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