A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180956



Internal ID20747996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76825698..76830427hg38UCSC Ensembl
chr17:74821780..74826509hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg384730
hg194730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180956
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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