A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936055



Internal ID21356124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38217260..38217416hg38UCSC Ensembl
chr22:38613267..38613423hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179504
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936055
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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