A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551557



Internal ID16338966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77926400..77927184hg38UCSC Ensembl
Innerchr10:79686158..79686942hg19UCSC Ensembl
Innerchr10:79356164..79356948hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38785
hg19785
hg18785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751739
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)nsv551557
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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