A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470018



Internal ID21127571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46335373..46336304hg38UCSC Ensembl
chr12:46729156..46730087hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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