A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193148



Internal ID20760188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10277556..10484931hg38UCSC Ensembl
chr10:10319519..10526894hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38207376
hg19207376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193148
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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