A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv746839



Internal ID16040795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35222966..35375528hg38UCSC Ensembl
Innerchr10:35511894..35664456hg19UCSC Ensembl
Innerchr10:35551900..35704462hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38152563
hg19152563
hg18152563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550403
Supporting Variants
Samples
Known GenesCCNY
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv746839
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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