A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545400



Internal ID20918631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23340679..24293165hg38UCSC Ensembl
chr22:23682866..24689133hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38952487
hg191006268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073539
Samples
Known GenesC22orf15, C22orf43, CABIN1, CES5AP1, CHCHD10, DDT, DDTL, DERL3, GGT5, GSTT1, GSTT2, GSTT2B, GSTTP1, GSTTP2, GUSBP11, IGLL1, LOC284889, LOC391322, MIF, MMP11, POM121L9P, RGL4, SLC2A11, SMARCB1, SPECC1L, SPECC1L-ADORA2A, SUSD2, VPREB3, ZDHHC8P1, ZNF70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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