A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421762



Internal ID21079315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39718701..39754500hg38UCSC Ensembl
chr8:39576220..39612019hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3835800
hg1935800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232009
Samples
Known GenesADAM18, ADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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