A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682936



Internal ID15072902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:147807005..148357730hg38UCSC Ensembl
Innerchr6:148128141..148678866hg19UCSC Ensembl
Innerchr6:148169834..148720559hg18UCSC Ensembl
Innerchr6:148169834..148720559hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38550726
hg19550726
hg18550726
hg17550726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520615
Supporting Variants
Samples
Known GenesSASH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682936
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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