A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343377



Internal ID21000930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22385480..22385874hg38UCSC Ensembl
chr2:22608352..22608746hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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