A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406064



Internal ID21063617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12012901..12023500hg38UCSC Ensembl
chr6:12013134..12023733hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214564
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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