A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907503



Internal ID22682712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161089890..161090681hg38UCSC Ensembl
chr3:160807678..160808469hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425658
Samples
Known GenesB3GALNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907503
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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