A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432431



Internal ID21089984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29781943..29871425hg38UCSC Ensembl
chr8:29639459..29728941hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3889483
hg1989483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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