A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619496



Internal ID21811543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40376514..40376597hg38UCSC Ensembl
chr17:38532766..38532849hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619496
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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