A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417623



Internal ID21075176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9028702..9031821hg38UCSC Ensembl
chr8:8886212..8889331hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383120
hg193120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173705
Samples
Known GenesERI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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