A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344326



Internal ID21001879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43189078..43191755hg38UCSC Ensembl
chr2:43416217..43418894hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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