A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523579



Internal ID15450872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52874219..53236498hg38UCSC Ensembl
Innerchr17:50951579..51313859hg19UCSC Ensembl
Innerchr17:48306578..48668858hg18UCSC Ensembl
Innerchr17:48306578..48668858hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38362280
hg19362281
hg18362281
hg17362281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699365
Samples
Known GenesC17orf112
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer