A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187554



Internal ID20754594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116983708..117003917hg38UCSC Ensembl
chr10:118743219..118763428hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3820210
hg1920210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438716
Supporting Variants
Samples
Known GenesKIAA1598
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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