A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552296



Internal ID16339705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:126698580..126880976hg38UCSC Ensembl
Innerchr10:128387149..128569545hg19UCSC Ensembl
Innerchr10:128377139..128559535hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38182397
hg19182397
hg18182397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n54
Supporting Variantsnssv1174581
Samples1780862224_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552296
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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