A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444926



Internal ID21102479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43451045..43463477hg38UCSC Ensembl
chr10:43946493..43958925hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812433
hg1912433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184498
Samples
Known GenesZNF487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444926
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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