A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316073



Internal ID20849150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47763882..47851784hg38UCSC Ensembl
chr1:48229554..48317456hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3887903
hg1987903
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201402
Samples
Known GenesTRABD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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