A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720044



Internal ID18671639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33632376..34611003hg38UCSC Ensembl
Innerchr17:31959395..32938022hg19UCSC Ensembl
Innerchr17:28983508..29962135hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38978628
hg19978628
hg18978628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061741
Supporting Variants
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3720044
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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