A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550591



Internal ID16338000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41832703..41883666hg38UCSC Ensembl
Innerchr10:42356543..42407506hg19UCSC Ensembl
Innerchr10:41676549..41727512hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3850964
hg1950964
hg1850964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1075n54
Supporting Variantsnssv747165, nssv747164, nssv747162, nssv747163
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550591
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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