A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526857



Internal ID15454150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68791287..68793818hg38UCSC Ensembl
Innerchr17:66787428..66789959hg19UCSC Ensembl
Innerchr17:64299023..64301554hg18UCSC Ensembl
Innerchr17:64299023..64301554hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg382532
hg192532
hg182532
hg172532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703215
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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