A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292530



Internal ID20501748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27004357..27004439hg38UCSC Ensembl
chr15:27249504..27249586hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744242
Supporting Variants
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292530
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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