A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178362



Internal ID20745402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32346001..32347600hg38UCSC Ensembl
chr10:32634929..32636528hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436591
Supporting Variants
Samples
Known GenesEPC1, LOC102031319
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0003


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