A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366868



Internal ID21024421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174056526..174058550hg38UCSC Ensembl
chr3:173774316..173776340hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382025
hg192025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097234
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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