A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431311



Internal ID21088864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42138981..42172661hg38UCSC Ensembl
chr8:41996499..42030179hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3833681
hg1933681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221805
Samples
Known GenesAP3M2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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