A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352427



Internal ID21009980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195554074..195563586hg38UCSC Ensembl
chr2:196418798..196428310hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg389513
hg199513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081906
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352427
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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