A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177855



Internal ID20744895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98930010..99483501hg38UCSC Ensembl
chr15:99473239..100023706hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38553492
hg19550468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496297
Supporting Variants
Samples
Known GenesHSP90B2P, IGF1R, LRRC28, PGPEP1L, SYNM, TTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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