A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522366



Internal ID15449659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78743768..78771909hg38UCSC Ensembl
Innerchr17:76739850..76767991hg19UCSC Ensembl
Innerchr17:74251445..74279586hg18UCSC Ensembl
Innerchr17:74251445..74279586hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3828142
hg1928142
hg1828142
hg1728142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695146
Samples
Known GenesCYTH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522366
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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