A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670663



Internal ID15060629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17514406..17862250hg38UCSC Ensembl
Innerchr6:17514637..17862481hg19UCSC Ensembl
Innerchr6:17622616..17970460hg18UCSC Ensembl
Innerchr6:17622616..17970460hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38347845
hg19347845
hg18347845
hg17347845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516012
Supporting Variants
Samples
Known GenesCAP2, FAM8A1, KIF13A, NUP153
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670663
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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