A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359844



Internal ID21017397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100823890..100824271hg38UCSC Ensembl
chr3:100542734..100543115hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091750
Samples
Known GenesABI3BP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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