A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353294



Internal ID21010847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68730398..68765224hg38UCSC Ensembl
chr2:68957530..68992356hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3834827
hg1934827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088857
Samples
Known GenesARHGAP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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