A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539302



Internal ID20912603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41476947..41492599hg38UCSC Ensembl
chr22:41872951..41888603hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3815653
hg1915653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074512
Samples
Known GenesACO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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