A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636232



Internal ID21828279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29062364..29066364hg38UCSC Ensembl
chr17:27389382..27393382hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636232
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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