A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485017



Internal ID262414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4961611..4965312hg38UCSC Ensembl
chr10:5003803..5007504hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg383702
hg193702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029544
Samples
Known GenesAKR1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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