A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967075



Internal ID22742010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35232177..35232177hg38UCSC Ensembl
chr9:35232174..35232174hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446932
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967075
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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