A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181607



Internal ID20748647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31690838..31702703hg38UCSC Ensembl
chr17:30017857..30029722hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3811866
hg1911866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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