A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543466



Internal ID20916714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23389632..24058869hg38UCSC Ensembl
chr22:23731819..24455332hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38669238
hg19723514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206733
Samples
Known GenesC22orf15, C22orf43, CABIN1, CHCHD10, DDT, DDTL, DERL3, GSTT1, GSTT2, GSTT2B, GSTTP1, GSTTP2, GUSBP11, IGLL1, LOC284889, LOC391322, MIF, MMP11, RGL4, SLC2A11, SMARCB1, VPREB3, ZDHHC8P1, ZNF70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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