A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396056



Internal ID21053609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106338603..106378933hg38UCSC Ensembl
chr5:105674304..105714634hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3840331
hg1940331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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