A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419632



Internal ID21077185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42981884..42992399hg38UCSC Ensembl
chr8:42837027..42847542hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810516
hg1910516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232183
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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