A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066757



Internal ID18809288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33630132..34608994hg38UCSC Ensembl
Innerchr17:31957151..32936013hg19UCSC Ensembl
Innerchr17:28981264..29960126hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38978863
hg19978863
hg18978863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3141n100
Supporting Variantsnssv3561064
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)nsv1066757
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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