A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550018



Internal ID16337427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16202095..16237016hg38UCSC Ensembl
Innerchr10:16244094..16279015hg19UCSC Ensembl
Innerchr10:16284100..16319021hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3834922
hg1934922
hg1834922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744101
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550018
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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