A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181165



Internal ID20748205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76821329..76856023hg38UCSC Ensembl
chr17:74817411..74852105hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3834695
hg1934695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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