A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654834



Internal ID15391486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101495005hg38UCSC Ensembl
Innerchr7:100968363..101138286hg19UCSC Ensembl
Innerchr7:100755083..100925006hg18UCSC Ensembl
Innerchr7:100561798..100731721hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38169924
hg19169924
hg18169924
hg17169924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517175
Supporting Variants
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654834
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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