A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459691



Internal ID21117244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66866426..67037930hg38UCSC Ensembl
chr12:67260206..67431710hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38171505
hg19171505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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