A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364544



Internal ID21022097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186879696..186968928hg38UCSC Ensembl
chr3:186597485..186686716hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3889233
hg1989232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212220
Samples
Known GenesST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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