A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416844



Internal ID21074397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100555701..100561300hg38UCSC Ensembl
chr8:101567929..101573528hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219135
Samples
Known GenesANKRD46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416844
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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