A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344853



Internal ID21002406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20031787..20041029hg38UCSC Ensembl
chr2:20231548..20240790hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389243
hg199243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083980
Samples
Known GenesLAPTM4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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