A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550210



Internal ID16337619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22723167..22775773hg38UCSC Ensembl
Innerchr10:23012096..23064702hg19UCSC Ensembl
Innerchr10:23052102..23104708hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3852607
hg1952607
hg1852607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744711
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550210
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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