A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624393



Internal ID21816440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40011423..40011543hg38UCSC Ensembl
chr17:38167676..38167796hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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