A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195761



Internal ID20762801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28305680..28306106hg38UCSC Ensembl
chr10:28594609..28595035hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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