A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362986



Internal ID21020539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140755313..140755831hg38UCSC Ensembl
chr3:140474155..140474673hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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