A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475972



Internal ID253599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8147416..8160584hg38UCSC Ensembl
chr10:8189379..8202547hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813169
hg1913169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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