A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528816



Internal ID15456109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9297098..9304136hg38UCSC Ensembl
Innerchr17:9200415..9207453hg19UCSC Ensembl
Innerchr17:9141140..9148178hg18UCSC Ensembl
Innerchr17:9141140..9148178hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
hg177039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705490
Samples
Known GenesSTX8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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