A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408018



Internal ID21065571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103520709..103529467hg38UCSC Ensembl
chr5:102856410..102865168hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg388759
hg198759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122649
Samples
Known GenesLOC102467212
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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