A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419613



Internal ID21077166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52930201..53029800hg38UCSC Ensembl
chr8:53842761..53942360hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3899600
hg1999600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226549
Samples
Known GenesNPBWR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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