A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907254



Internal ID22682460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185876571..185880058hg38UCSC Ensembl
chr3:185594359..185597846hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383488
hg193488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907254
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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