A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549800



Internal ID16337209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2382612..2504830hg38UCSC Ensembl
Innerchr10:2424806..2547022hg19UCSC Ensembl
Innerchr10:2414806..2537022hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38122219
hg19122217
hg18122217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740234
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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