A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551744



Internal ID16339153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83187390..83189286hg38UCSC Ensembl
Innerchr10:84947146..84949042hg19UCSC Ensembl
Innerchr10:84937126..84939022hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381897
hg191897
hg181897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv752136
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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