A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383559



Internal ID22441429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34751955..34751955hg38UCSC Ensembl
chr15:35044156..35044156hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972588
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383559
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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