A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487704



Internal ID265036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70776075..70776516hg38UCSC Ensembl
chr10:72535831..72536272hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037480
Samples
Known GenesTBATA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487704
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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