A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420174



Internal ID21077727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63035101..63042800hg38UCSC Ensembl
chr8:63947660..63955359hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223389
Samples
Known GenesGGH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420174
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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