A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385373



Internal ID21042926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111406101..111409300hg38UCSC Ensembl
chr4:112327257..112330456hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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