A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551556



Internal ID16338965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77926348..77927131hg38UCSC Ensembl
Innerchr10:79686106..79686889hg19UCSC Ensembl
Innerchr10:79356112..79356895hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38784
hg19784
hg18784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1272n54
Supporting Variantsnssv751738
Samples
Known GenesDLG5, DLG5-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551556
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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