A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440293



Internal ID21097846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137842701..138191300hg38UCSC Ensembl
chr9:140737153..141085752hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38348600
hg19348600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228707
Samples
Known GenesCACNA1B, TUBBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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