A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539005



Internal ID20912312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37727973..37738961hg38UCSC Ensembl
chr22:38123980..38134968hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810989
hg1910989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073924
Samples
Known GenesTRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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