A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961753



Internal ID22736695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22343726..22918246hg38UCSC Ensembl
chr22:22698078..23260418hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38574521
hg19562341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1383n209
Supporting Variantsnssv17408733
Samples
Known GenesGGTLC2, IGLL5, LOC648691, MIR650, POM121L1P, PRAME, ZNF280A, ZNF280B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961753
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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