A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703881



Internal ID15440533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:31718205..31729919hg38UCSC Ensembl
Innerchr17:30045224..30056938hg19UCSC Ensembl
Innerchr17:27069337..27081051hg18UCSC Ensembl
Innerchr17:27069337..27081051hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3811715
hg1911715
hg1811715
hg1711715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527440
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703881
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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