A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516735



Internal ID15444028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69743613..69762154hg38UCSC Ensembl
Innerchr17:67739754..67758295hg19UCSC Ensembl
Innerchr17:65251349..65269890hg18UCSC Ensembl
Innerchr17:65251349..65269890hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3818542
hg1918542
hg1818542
hg1718542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686993, nssv670535, nssv676549
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516735
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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