A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189743



Internal ID20756783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7956285..7956741hg38UCSC Ensembl
chr17:7859603..7860059hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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