A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187852



Internal ID20754892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33564039..33577423hg38UCSC Ensembl
chr10:33852967..33866351hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3813385
hg1913385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00171


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