A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551536



Internal ID15992259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74825347..74827100hg38UCSC Ensembl
Innerchr10:76585105..76586858hg19UCSC Ensembl
Innerchr10:76255111..76256864hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381754
hg191754
hg181754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv750294
Samples
Known GenesKAT6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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