A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899653



Internal ID22674785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137615671..137619439hg38UCSC Ensembl
chr4:138536825..138540593hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg383769
hg193769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899653
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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