A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442912



Internal ID21100465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4859877..5282828hg38UCSC Ensembl
chr10:4902069..5324791hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38422952
hg19422723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv601n223
Supporting Variantsnssv17979989
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1C6P, AKR1CL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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