A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428435



Internal ID21085988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56993401..56998700hg38UCSC Ensembl
chr8:57905960..57911259hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225344
Samples
Known GenesIMPAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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