A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412922



Internal ID21070475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142854907..142859691hg38UCSC Ensembl
chr5:142234472..142239256hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg384785
hg194785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125859
Samples
Known GenesARHGAP26, ARHGAP26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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