A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664310



Internal ID15054276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34320812..34359191hg38UCSC Ensembl
Innerchr17:32647831..32686210hg19UCSC Ensembl
Innerchr17:29671944..29710323hg18UCSC Ensembl
Innerchr17:29671944..29710323hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3838380
hg1938380
hg1838380
hg1738380
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)nssv664310
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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