A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367493



Internal ID21025046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174032263..174279066hg38UCSC Ensembl
chr3:173750053..173996856hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38246804
hg19246804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097229
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367493
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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