A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636680



Internal ID21828727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55457587..55457656hg38UCSC Ensembl
chr17:53534948..53535017hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636680
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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