A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354281



Internal ID21011834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231353267..231365807hg38UCSC Ensembl
chr2:232217979..232230518hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3812541
hg1912540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086573
Samples
Known GenesARMC9, MIR4777
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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