A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674463



Internal ID15411115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101317269..101484174hg38UCSC Ensembl
Innerchr7:100960550..101127455hg19UCSC Ensembl
Innerchr7:100747270..100914175hg18UCSC Ensembl
Innerchr7:100553985..100720890hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38166906
hg19166906
hg18166906
hg17166906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517175
Supporting Variants
Samples
Known GenesCOL26A1, RABL5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674463
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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