A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184712



Internal ID20751752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33059528..33061499hg38UCSC Ensembl
chr10:33348456..33350427hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381972
hg191972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184712
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00097


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