A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340675



Internal ID20998228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24517147..24525352hg38UCSC Ensembl
chr2:24740016..24748221hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg388206
hg198206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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