A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034602



Internal ID90779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47468265..47498265hg38UCSC Ensembl
chr10:48241097..48271097hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143251
Supporting Variants
Samples
Known GenesANXA8, FAM25C, FAM25G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.025261


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