A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621503



Internal ID21813550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48844668..48844729hg38UCSC Ensembl
chr17:46922030..46922091hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030149
Supporting Variants
Samples
Known GenesCALCOCO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621503
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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