A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340695



Internal ID20998248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5639848..5652173hg38UCSC Ensembl
chr2:5779980..5792305hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3812326
hg1912326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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