A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913920



Internal ID22689136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66044455..66044514hg38UCSC Ensembl
chr8:66956690..66956749hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432744
Samples
Known GenesDNAJC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913920
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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