A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433678



Internal ID21091231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50529530..50566586hg38UCSC Ensembl
chr8:51442090..51479146hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3837057
hg1937057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220983
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433678
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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