A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329906



Internal ID20863059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154302732..154337071hg38UCSC Ensembl
chr1:154275208..154309547hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3834340
hg1934340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200503
Samples
Known GenesAQP10, ATP8B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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