A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420877



Internal ID21078430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17245001..17249800hg38UCSC Ensembl
chr8:17102510..17107309hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232232
Samples
Known GenesCNOT7, VPS37A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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