A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434047



Internal ID21091600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132831514..132832271hg38UCSC Ensembl
chr8:133843759..133844516hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165717
Samples
Known GenesPHF20L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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