A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552096



Internal ID16339505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105360399..105535424hg38UCSC Ensembl
Innerchr10:107120157..107295182hg19UCSC Ensembl
Innerchr10:107110147..107285172hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38175026
hg19175026
hg18175026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1377n54
Supporting Variantsnssv1174572
Samples1780862414_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552096
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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