A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550545



Internal ID16337954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38782022..38855767hg38UCSC Ensembl
Innerchr10:39075153..39148898hg19UCSC Ensembl
Innerchr10:39115159..39188904hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3873746
hg1973746
hg1873746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1065n54
Supporting Variantsnssv747041, nssv747042
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550545
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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