A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456344



Internal ID21113897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81676071..81676802hg38UCSC Ensembl
chr12:82069850..82070581hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18004200
Samples
Known GenesPPFIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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