A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369385



Internal ID21026938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119321016..119321325hg38UCSC Ensembl
chr3:119039863..119040172hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094548
Samples
Known GenesARHGAP31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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