A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194064



Internal ID20761104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21275637..21280639hg38UCSC Ensembl
chr10:21564566..21569568hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385003
hg195003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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