A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023729



Internal ID20590769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27412273..27412643hg38UCSC Ensembl
chr15:27657419..27657789hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505998
Supporting Variants
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00095


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