A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344845



Internal ID21002398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165679601..165700800hg38UCSC Ensembl
chr2:166536111..166557310hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3821200
hg1921200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4177n223
Supporting Variantsnssv18081241
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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