A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404297



Internal ID21061850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103409601..103464900hg38UCSC Ensembl
chr5:102745302..102800601hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3855300
hg1955300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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