A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550596



Internal ID16338005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41773083..41877498hg38UCSC Ensembl
Innerchr10:42362711..42467126hg19UCSC Ensembl
Innerchr10:41682717..41787132hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38104416
hg19104416
hg18104416
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1076n54
Supporting Variantsnssv747171
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550596
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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