A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444614



Internal ID21102167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17443862..17444228hg38UCSC Ensembl
chr10:17485861..17486227hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978979
Samples
Known GenesST8SIA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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