A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425811



Internal ID21083364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39305089..39317527hg38UCSC Ensembl
chr8:39162608..39175046hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3812439
hg1912439
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221913
Samples
Known GenesADAM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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