A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149678



Internal ID15509088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4102227..4170104hg38UCSC Ensembl
Innerchr17:4005521..4073398hg19UCSC Ensembl
Innerchr17:3952270..4020147hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3867878
hg1967878
hg1867878
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574266
Supporting Variants
Samples1782681317_A
Known GenesANKFY1, CYB5D2, ZZEF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149678
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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