A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476052



Internal ID253674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91409429..91409503hg38UCSC Ensembl
chr10:93169186..93169260hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036895
Samples
Known GenesLOC100188947
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476052
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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