A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552101



Internal ID16339510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105865495..105921689hg38UCSC Ensembl
Innerchr10:107625253..107681447hg19UCSC Ensembl
Innerchr10:107615243..107671437hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3856195
hg1956195
hg1856195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1379n54
Supporting Variantsnssv1174573, nssv756251, nssv756250
Samples1780862444_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552101
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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