A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536174



Internal ID20909529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25446715..25642171hg38UCSC Ensembl
chr22:25842682..26038138hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38195457
hg19195457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074143
Samples
Known GenesADRBK2, CRYBB2P1, MIR6817
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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