A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190161



Internal ID20757201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104592781..104594131hg38UCSC Ensembl
chr10:106352539..106353889hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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