A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369967



Internal ID21027520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68656810..68657050hg38UCSC Ensembl
chr3:68705961..68706201hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369967
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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