A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385592



Internal ID21043145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119996901..119999500hg38UCSC Ensembl
chr4:120918056..120920655hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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