A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371937



Internal ID21029490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140589587..140594195hg38UCSC Ensembl
chr3:140308429..140313037hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg384609
hg194609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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