A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751737



Internal ID16045693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77926193..77926785hg38UCSC Ensembl
Innerchr10:79685951..79686543hg19UCSC Ensembl
Innerchr10:79355957..79356549hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551555
Supporting Variants
Samples
Known GenesDLG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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