A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165559



Internal ID20732599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144535540..144545322hg38UCSC Ensembl
chr8:145760924..145770706hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg389783
hg199783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429293
Supporting Variants
Samples
Known GenesARHGAP39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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