A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6388031



Internal ID21045584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119994084..119999658hg38UCSC Ensembl
chr4:120915239..120920813hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg385575
hg195575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5434n223
Supporting Variantsnssv18107812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6388031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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