A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474107



Internal ID21131660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18851989..18853354hg38UCSC Ensembl
chr12:19004923..19006288hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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