A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360189



Internal ID21017742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58952959..58953552hg38UCSC Ensembl
chr3:58938685..58939278hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103502
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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