A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415044



Internal ID21072597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13129701..13137900hg38UCSC Ensembl
chr6:13129933..13138132hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215557
Samples
Known GenesPHACTR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415044
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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