A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399305



Internal ID21056858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106267575..106390193hg38UCSC Ensembl
chr5:105603276..105725894hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38122619
hg19122619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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