A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518133



Internal ID15445426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8106586..8106910hg38UCSC Ensembl
Innerchr17:8009904..8010228hg19UCSC Ensembl
Innerchr17:7950629..7950953hg18UCSC Ensembl
Innerchr17:7950629..7950953hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38325
hg19325
hg18325
hg17325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695549
Samples
Known GenesALOXE3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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