A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348197



Internal ID21005750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215269574..215274030hg38UCSC Ensembl
chr2:216134297..216138753hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg384457
hg194457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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