A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979989



Internal ID20547029
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 StatusS
Merged Variantsnsv6442912
Supporting Variants
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1C6P, AKR1CL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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