A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356043



Internal ID21013596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100862117..100866389hg38UCSC Ensembl
chr3:100580961..100585233hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg384273
hg194273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091754
Samples
Known GenesABI3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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