A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901537



Internal ID22676688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138171024..138171396hg38UCSC Ensembl
chr6:138492161..138492533hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420785
Samples
Known GenesKIAA1244
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901537
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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