A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543371



Internal ID20916619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24773986..24836945hg38UCSC Ensembl
chr22:25169953..25232912hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3862960
hg1962960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073450
Samples
Known GenesPIWIL3, SGSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543371
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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