A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458256



Internal ID21115809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:58903469..58904789hg38UCSC Ensembl
chr12:59297250..59298570hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002062
Samples
Known GenesLRIG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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