A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907363



Internal ID22682571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87960128..87960213hg38UCSC Ensembl
chr3:88009278..88009363hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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