A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550179



Internal ID16337588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20561695..20588852hg38UCSC Ensembl
Innerchr10:20850624..20877781hg19UCSC Ensembl
Innerchr10:20890630..20917787hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3827158
hg1927158
hg1827158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv994n54
Supporting Variantsnssv1173860
SamplesNINDS_84
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550179
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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