A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395514



Internal ID21053067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85676359..85682159hg38UCSC Ensembl
chr4:86597512..86603312hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg385801
hg195801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121656
Samples
Known GenesARHGAP24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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