A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616627



Internal ID20989698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167282324..167373532hg38UCSC Ensembl
chr6:167695812..167787020hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3891209
hg1991209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217048
Samples
Known GenesTCP10, TTLL2, UNC93A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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