A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899008



Internal ID22674133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55796597..55802462hg38UCSC Ensembl
chr4:56662763..56668628hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385866
hg195866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899008
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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