A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550542



Internal ID16337951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38597109..38680369hg38UCSC Ensembl
Innerchr10:38890240..38973500hg19UCSC Ensembl
Innerchr10:38930246..39013506hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3883261
hg1983261
hg1883261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1052n54
Supporting Variantsnssv747038
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550542
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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