A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552100



Internal ID16339509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105852798..105922177hg38UCSC Ensembl
Innerchr10:107612556..107681935hg19UCSC Ensembl
Innerchr10:107602546..107671925hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3869380
hg1969380
hg1869380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1379n54
Supporting Variantsnssv756249
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552100
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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