A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550607



Internal ID16338016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41813135..41861510hg38UCSC Ensembl
Innerchr10:42378699..42427074hg19UCSC Ensembl
Innerchr10:41698705..41747080hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3848376
hg1948376
hg1848376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1080n54
Supporting Variantsnssv747183
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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