A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15187535



Internal ID21326373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167056594..167056594hg38UCSC Ensembl
chr1:167025831..167025831hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381115
hg191115
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935533
Supporting Variants
SamplesHG002
Known GenesGPA33
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15187535
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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