A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517895



Internal ID15445188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72761686..72993562hg38UCSC Ensembl
Innerchr17:70757825..70989701hg19UCSC Ensembl
Innerchr17:68269420..68501296hg18UCSC Ensembl
Innerchr17:68269420..68501296hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38231877
hg19231877
hg18231877
hg17231877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695304
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517895
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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