A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889233



Internal ID22664248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173646995..173659643hg38UCSC Ensembl
chr3:173364785..173377433hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3812649
hg1912649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423323
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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