A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550124



Internal ID16337533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18916174..19018607hg38UCSC Ensembl
Innerchr10:19205103..19307536hg19UCSC Ensembl
Innerchr10:19245109..19347542hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38102434
hg19102434
hg18102434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174141
SamplesHGDP01406
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550124
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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