A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382082



Internal ID21039635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87142267..87150495hg38UCSC Ensembl
chr4:88063419..88071647hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg388229
hg198229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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