A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187410



Internal ID21326243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35673756..35673756hg38UCSC Ensembl
chr22:36069803..36069803hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944492
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187410
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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