A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352182



Internal ID21009735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23222629..23224645hg38UCSC Ensembl
chr2:23445500..23447516hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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