A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898981



Internal ID22674106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173734533..173735669hg38UCSC Ensembl
chr3:173452323..173453459hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429396
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898981
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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