A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703595



Internal ID21375871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133011042..133011201hg38UCSC Ensembl
chr5:132346734..132346893hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392123
Supporting Variants
Samples
Known GenesZCCHC10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703595
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.112069


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