A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023726



Internal ID20590766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27365027..27368036hg38UCSC Ensembl
chr15:27610173..27613182hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg383010
hg193010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514149
Supporting Variants
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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