A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097263



Internal ID20664303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174282259..174282648hg38UCSC Ensembl
chr3:174000049..174000438hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357723
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00153


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