A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609772



Internal ID21801819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34059031..34059166hg38UCSC Ensembl
chr15:34351232..34351367hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023330
Supporting Variants
Samples
Known GenesCHRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609772
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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