A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396865



Internal ID21054418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143094769..143096960hg38UCSC Ensembl
chr5:142474334..142476525hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125864
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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