A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550590



Internal ID16337999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:41838960..41883666hg38UCSC Ensembl
Innerchr10:42356543..42401249hg19UCSC Ensembl
Innerchr10:41676549..41721255hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3844707
hg1944707
hg1844707
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1075n54
Supporting Variantsnssv747158, nssv747161, nssv747157, nssv747160, nssv747159
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550590
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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