A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468273



Internal ID21125826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106041120..106043190hg38UCSC Ensembl
chr12:106434898..106436968hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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