A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179972



Internal ID20747012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28033708..28212053hg38UCSC Ensembl
chr10:28322637..28500982hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38178346
hg19178346
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449018
Supporting Variants
Samples
Known GenesMPP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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