A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550592



Internal ID16338001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41818724..41883666hg38UCSC Ensembl
Innerchr10:42356543..42421485hg19UCSC Ensembl
Innerchr10:41676549..41741491hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3864943
hg1964943
hg1864943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv747166, nssv747167
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550592
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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