A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186408



Internal ID20753448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43891675..43903473hg38UCSC Ensembl
chr17:41969043..41980841hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3811799
hg1911799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514543
Supporting Variants
Samples
Known GenesMPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186408
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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