A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422740



Internal ID21080293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41860077..41900629hg38UCSC Ensembl
chr8:41717595..41758147hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3840553
hg1940553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232180
Samples
Known GenesANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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