A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401428



Internal ID21058981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83183069..83218979hg38UCSC Ensembl
chr5:82478888..82514798hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3835911
hg1935911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133040
Samples
Known GenesXRCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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