A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625723



Internal ID21817770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70086695..70086910hg38UCSC Ensembl
chr17:68082836..68083051hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025046
Supporting Variants
Samples
Known GenesKCNJ16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625723
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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