A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896457



Internal ID22671550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65031330..65031395hg38UCSC Ensembl
chr3:65017005..65017070hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896457
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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