A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360843



Internal ID21018396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57521042..57523711hg38UCSC Ensembl
chr3:57506769..57509438hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg382670
hg192670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102901
Samples
Known GenesDNAH12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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