A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345343



Internal ID21002896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165780622..165783379hg38UCSC Ensembl
chr2:166637132..166639889hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg382758
hg192758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081249
Samples
Known GenesGALNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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