A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445132



Internal ID21102685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89475933..89476514hg38UCSC Ensembl
chr10:91235690..91236271hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984960
Samples
Known GenesSLC16A12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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