A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186287



Internal ID20753328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57669052..57677254hg38UCSC Ensembl
chr10:59428812..59437014hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg388203
hg198203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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