A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352945



Internal ID21010498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26799585..26802422hg38UCSC Ensembl
chr2:27022453..27025290hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382838
hg192838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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