A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454592



Internal ID21112145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83701101..83739300hg38UCSC Ensembl
chr9:86316016..86354215hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3838200
hg1938200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228082
Samples
Known GenesUBQLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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