A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550598



Internal ID16338007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41838960..41877078hg38UCSC Ensembl
Innerchr10:42363131..42401249hg19UCSC Ensembl
Innerchr10:41683137..41721255hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3838119
hg1938119
hg1838119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1078n54
Supporting Variantsnssv747173
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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