A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522835



Internal ID15103442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36084845..36153146hg38UCSC Ensembl
Innerchr17:34412202..34480526hg19UCSC Ensembl
Innerchr17:31436315..31504639hg18UCSC Ensembl
Innerchr17:31436315..31504639hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3868302
hg1968325
hg1868325
hg1768325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv178n21
Supporting Variantsnssv698486
Samples
Known GenesCCL3, CCL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522835
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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