A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475067



Internal ID21132620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34186392..34190913hg38UCSC Ensembl
chr11:34207939..34212460hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384522
hg194522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990832
Samples
Known GenesABTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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