A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195797



Internal ID20762837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78210163..78218091hg38UCSC Ensembl
chr17:76206244..76214172hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387929
hg197929
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535006
Supporting Variants
Samples
Known GenesBIRC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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