A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522084



Internal ID298358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11173327..11173433hg38UCSC Ensembl
chr19:11284003..11284109hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721381
Samples
Known GenesKANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522084
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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