A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599043



Internal ID21791088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70376563..70376563hg38UCSC Ensembl
chr15:70668902..70668902hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083634
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599043
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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