A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341149



Internal ID20998702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21000518..21022373hg38UCSC Ensembl
chr2:21223390..21245245hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3821856
hg1921856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085099
Samples
Known GenesAPOB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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