A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747168



Internal ID16041124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41795035..41883666hg38UCSC Ensembl
Innerchr10:42356543..42445174hg19UCSC Ensembl
Innerchr10:41676549..41765180hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3888632
hg1988632
hg1888632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550593
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747168
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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