A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177251



Internal ID20744291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100773958..100774570hg38UCSC Ensembl
chr15:101314163..101314775hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502890
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177251
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00229


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