A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622911



Internal ID21814958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60551708..60551761hg38UCSC Ensembl
chr17:58629069..58629122hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622911
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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