A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034647



Internal ID90812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50014026..50024368hg38UCSC Ensembl
chr10:51773786..51784128hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3810343
hg1910343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143218
Supporting Variants
Samples
Known GenesFLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034647
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.024126


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