A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185992



Internal ID20753032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44991294..45019856hg38UCSC Ensembl
chr10:45486742..45515304hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3828563
hg1928563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442634
Supporting Variants
Samples
Known GenesC10orf25, RASSF4, ZNF22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185992
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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