A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429367



Internal ID21086920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144588001..144593200hg38UCSC Ensembl
chr8:145813385..145818584hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165561
Samples
Known GenesARHGAP39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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