A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518722



Internal ID15446015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77862451..77865571hg38UCSC Ensembl
Innerchr17:75858533..75861653hg19UCSC Ensembl
Innerchr17:73370128..73373248hg18UCSC Ensembl
Innerchr17:73370128..73373248hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383121
hg193121
hg183121
hg173121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696172
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518722
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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