A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474499



Internal ID21132052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60203704..60204379hg38UCSC Ensembl
chr12:60597485..60598160hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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