A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346943



Internal ID21004496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166501535..166502043hg38UCSC Ensembl
chr2:167358045..167358553hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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