A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550127



Internal ID16337536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19031864..19056050hg38UCSC Ensembl
Innerchr10:19320793..19344979hg19UCSC Ensembl
Innerchr10:19360799..19384985hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3824187
hg1924187
hg1824187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744283
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550127
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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