A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890003



Internal ID22665027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36976821..36985796hg38UCSC Ensembl
chr4:36978443..36987418hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388976
hg198976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890003
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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