A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632075



Internal ID21824122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48854128..48854244hg38UCSC Ensembl
chr17:46931490..46931606hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031186
Supporting Variants
Samples
Known GenesCALCOCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632075
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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