A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195706



Internal ID20762746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47944101..47948900hg38UCSC Ensembl
chr10:47109204..47113998hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384800
hg194795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449239
Supporting Variants
Samples
Known GenesLINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.16783


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