A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181506



Internal ID20748546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28821152..28857573hg38UCSC Ensembl
chr10:29110081..29146502hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3836422
hg1936422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441577
Supporting Variants
Samples
Known GenesC10orf126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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