A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747288



Internal ID15694558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42230215..42594517hg38UCSC Ensembl
Innerchr10:42725663..43089965hg19UCSC Ensembl
Innerchr10:42045669..42409971hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38364303
hg19364303
hg18364303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550670
Supporting Variants
Samples
Known GenesCCNYL2, LINC00839, LOC441666, ZNF33B, ZNF37BP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747288
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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