A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605951



Internal ID21797998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34018843..34018910hg38UCSC Ensembl
chr15:34311044..34311111hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028930
Supporting Variants
Samples
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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