A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019352



Internal ID21928695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42840842..42840920hg38UCSC Ensembl
chr8:42695985..42696063hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579958
Samples
Known GenesTHAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019352
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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