A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014032



Internal ID21923375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4929820..5080261hg38UCSC Ensembl
chr10:4972012..5122453hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38150442
hg19150442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588478
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014032
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer