A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467072



Internal ID21124625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79611001..79612500hg38UCSC Ensembl
chr12:80004781..80006280hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003809
Samples
Known GenesPAWR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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