A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178679



Internal ID20745719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98955540..99303731hg38UCSC Ensembl
chr15:99498769..99843936hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38348192
hg19345168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509935
Supporting Variants
Samples
Known GenesHSP90B2P, IGF1R, LRRC28, PGPEP1L, SYNM, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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