A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177865



Internal ID20744905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92396254..92400263hg38UCSC Ensembl
chr10:94156011..94160020hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg384010
hg194010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453815
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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