A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377890



Internal ID21035443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102817758..102818259hg38UCSC Ensembl
chr4:103738915..103739416hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107500
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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