A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469121



Internal ID21126674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106907466..106914629hg38UCSC Ensembl
chr12:107301244..107308407hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg387164
hg197164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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