A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525599



Internal ID8419874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63480868..63482562hg38UCSC Ensembl
Innerchr17:61558229..61559923hg19UCSC Ensembl
Innerchr17:58911961..58913655hg18UCSC Ensembl
Innerchr17:58911961..58913655hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381695
hg191695
hg181695
hg171695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701742
Samples
Known GenesACE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525599
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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