A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526477



Internal ID15107084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77499315..77500378hg38UCSC Ensembl
Innerchr17:75495397..75496460hg19UCSC Ensembl
Innerchr17:73006992..73008055hg18UCSC Ensembl
Innerchr17:73006992..73008055hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381064
hg191064
hg181064
hg171064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702784
Samples
Known GenesSEPT9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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