A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536773



Internal ID20910116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38168642..38169996hg38UCSC Ensembl
chr22:38564649..38566003hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073946
Samples
Known GenesPLA2G6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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