A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344843



Internal ID21002396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9772023..9795245hg38UCSC Ensembl
chr2:9912152..9935374hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3823223
hg1923223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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