A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348445



Internal ID21005998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20701696..20714173hg38UCSC Ensembl
chr2:20901456..20913933hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3812478
hg1912478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082556
Samples
Known GenesC2orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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