A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409657



Internal ID21067210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52675894..52677285hg38UCSC Ensembl
chr6:52540692..52542083hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233812
Samples
Known GenesTMEM14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409657
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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