A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549763



Internal ID16337172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:586808..634488hg38UCSC Ensembl
Innerchr10:632748..680428hg19UCSC Ensembl
Innerchr10:622748..670428hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3847681
hg1947681
hg1847681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174095
SamplesHGDP00811
Known GenesDIP2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549763
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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