A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517262



Internal ID15097869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36104732..36153146hg38UCSC Ensembl
Innerchr17:34432125..34480526hg19UCSC Ensembl
Innerchr17:31456238..31504639hg18UCSC Ensembl
Innerchr17:31456238..31504639hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3848415
hg1948402
hg1848402
hg1748402
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667638, nssv699714, nssv665437, nssv654155, nssv670097, nssv686897, nssv665147, nssv652688, nssv658654
Samples
Known GenesCCL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517262
Frequency
Sample Size2026
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


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