A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401203



Internal ID21058756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34804449..34858590hg38UCSC Ensembl
chr6:34772226..34826367hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3854142
hg1954142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219594
Samples
Known GenesUHRF1BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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