A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190895



Internal ID20757935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26822101..26896600hg38UCSC Ensembl
chr15:27067248..27141747hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3874500
hg1974500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507248
Supporting Variants
Samples
Known GenesGABRA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190895
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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