A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445044



Internal ID21102597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107157933..107194859hg38UCSC Ensembl
chr10:108917691..108954617hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3836927
hg1936927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183211
Samples
Known GenesSORCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445044
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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