A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550151



Internal ID16337560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20489512..20525654hg38UCSC Ensembl
Innerchr10:20778441..20814583hg19UCSC Ensembl
Innerchr10:20818447..20854589hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3836143
hg1936143
hg1836143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv990n54
Supporting Variantsnssv744324, nssv1174148, nssv744325, nssv744326
Samples1780862431_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550151
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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