A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432391



Internal ID21089944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105316701..105319900hg38UCSC Ensembl
chr8:106328929..106332128hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233899
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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