A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905587



Internal ID22680775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26056040..26056606hg38UCSC Ensembl
chr4:26057662..26058228hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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