A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194517



Internal ID20761557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67738901..67745400hg38UCSC Ensembl
chr10:69498659..69505158hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0017


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