A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336432



Internal ID20993985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36616436..36625205hg38UCSC Ensembl
chr2:36843579..36852348hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg388770
hg198770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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