A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701074



Internal ID15437726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62670618..62692442hg38UCSC Ensembl
Innerchr17:60747979..60769803hg19UCSC Ensembl
Innerchr17:58101711..58123535hg18UCSC Ensembl
Innerchr17:58101711..58123535hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3821825
hg1921825
hg1821825
hg1721825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516921
Supporting Variants
Samples
Known GenesMRC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701074
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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