A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422995



Internal ID21080548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38035321..38035813hg38UCSC Ensembl
chr8:37892839..37893331hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168922
Samples
Known GenesEIF4EBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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