A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659984



Internal ID15396636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78582226..78599049hg38UCSC Ensembl
Innerchr17:76578308..76595131hg19UCSC Ensembl
Innerchr17:74089903..74106726hg18UCSC Ensembl
Innerchr17:74089903..74106726hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3816824
hg1916824
hg1816824
hg1716824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515872
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659984
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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