A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413112



Internal ID21070665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132906164..132907760hg38UCSC Ensembl
chr5:132241856..132243452hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg381597
hg191597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127148
Samples
Known GenesAFF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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