A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360733



Internal ID21018286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147536419..147542824hg38UCSC Ensembl
chr3:147254206..147260611hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg386406
hg196406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360733
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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