A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349291



Internal ID21006844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165657141..165657524hg38UCSC Ensembl
chr2:166513651..166514034hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081239
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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