A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660932



Internal ID15050898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34320525..34358987hg38UCSC Ensembl
Innerchr17:32647544..32686006hg19UCSC Ensembl
Innerchr17:29671657..29710119hg18UCSC Ensembl
Innerchr17:29671657..29710119hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3838463
hg1938463
hg1838463
hg1738463
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517423
Supporting Variants
Samples
Known GenesCCL13, CCL8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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