A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516815



Internal ID15444108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71109443..71112612hg38UCSC Ensembl
Innerchr17:69105584..69108753hg19UCSC Ensembl
Innerchr17:66617179..66620348hg18UCSC Ensembl
Innerchr17:66617179..66620348hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383170
hg193170
hg183170
hg173170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658067, nssv672732, nssv693408, nssv671122, nssv681623
Samples
Known GenesCASC17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516815
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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