A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180367



Internal ID20747407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112180001..112188400hg38UCSC Ensembl
chr10:113939759..113948158hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445245
Supporting Variants
Samples
Known GenesGPAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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