A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481782



Internal ID259251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4881150..4881226hg38UCSC Ensembl
chr10:4923342..4923418hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029535
Samples
Known GenesAKR1C6P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481782
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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