A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418092



Internal ID21075645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123696027..123697028hg38UCSC Ensembl
chr8:124708267..124709268hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164016
Samples
Known GenesANXA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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