A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468465



Internal ID21126018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78615992..78616372hg38UCSC Ensembl
chr12:79009772..79010152hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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