A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515953



Internal ID15443010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:55856592..55859963hg38UCSC Ensembl
Innerchr17:53933953..53937324hg19UCSC Ensembl
Innerchr17:51288952..51292323hg18UCSC Ensembl
Innerchr17:51288952..51292323hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383372
hg193372
hg183372
hg173372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677866, nssv665439, nssv681303, nssv682906
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515953
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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