A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550632



Internal ID16338041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42155274..42325358hg38UCSC Ensembl
Innerchr10:42650722..42820806hg19UCSC Ensembl
Innerchr10:41970728..42140812hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38170085
hg19170085
hg18170085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088n54
Supporting Variantsnssv747215
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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