A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200285



Internal ID20767325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10010311..10016487hg38UCSC Ensembl
chr1:10070369..10076545hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg386177
hg196177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334461
Supporting Variants
Samples
Known GenesRBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200285
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00262


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