A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484886



Internal ID21142439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121979860..121982586hg38UCSC Ensembl
chr12:122417766..122420492hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382727
hg192727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997826
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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