A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422792



Internal ID21080345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39646501..39716600hg38UCSC Ensembl
chr8:39504020..39574119hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3870100
hg1970100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234089
Samples
Known GenesADAM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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