A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418680



Internal ID21076233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39492501..39638000hg38UCSC Ensembl
chr8:39350020..39495519hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38145500
hg19145500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232206
Samples
Known GenesADAM18, ADAM3A, LOC100130964
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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