A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549856



Internal ID16337265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3819022..3825610hg38UCSC Ensembl
Innerchr10:3861214..3867802hg19UCSC Ensembl
Innerchr10:3851214..3857802hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg386589
hg196589
hg186589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740479
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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