A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188254



Internal ID20755294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11888088..11902322hg38UCSC Ensembl
chr10:11930087..11944321hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3814235
hg1914235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444750
Supporting Variants
Samples
Known GenesPROSER2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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