A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421097



Internal ID21078650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119562396..119963335hg38UCSC Ensembl
chr8:120574636..120975575hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38400940
hg19400940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223561
Samples
Known GenesDEPTOR, DSCC1, ENPP2, TAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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