A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552239



Internal ID16339648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121676732..121701552hg38UCSC Ensembl
Innerchr10:123436246..123461066hg19UCSC Ensembl
Innerchr10:123426236..123451056hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3824821
hg1924821
hg1824821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1406n54
Supporting Variantsnssv760303, nssv760306, nssv760304, nssv760305
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552239
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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