A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066651



Internal ID18809182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4269648..4303948hg38UCSC Ensembl
Innerchr17:4172943..4207243hg19UCSC Ensembl
Innerchr17:4119692..4153992hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3834301
hg1934301
hg1834301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560125
Samples
Known GenesUBE2G1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066651
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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