A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384457



Internal ID21042010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115315413..115475606hg38UCSC Ensembl
chr4:116236569..116396762hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38160194
hg19160194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107065
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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