A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188674



Internal ID20755714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47820543..47821403hg38UCSC Ensembl
chr17:45897909..45898769hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515882
Supporting Variants
Samples
Known GenesOSBPL7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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