A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527058



Internal ID15107665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59378931..59388543hg38UCSC Ensembl
Innerchr17:57456292..57465904hg19UCSC Ensembl
Innerchr17:54811074..54820686hg18UCSC Ensembl
Innerchr17:54811074..54820686hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg389613
hg199613
hg189613
hg179613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703435
Samples
Known GenesYPEL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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