A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133028



Internal ID20700068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83115501..83180800hg38UCSC Ensembl
chr5:82411320..82476619hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3865300
hg1965300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409085
Supporting Variants
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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