A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485131



Internal ID262527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15603904..15761140hg38UCSC Ensembl
chr10:15645903..15803139hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38157237
hg19157237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032107
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485131
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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