A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912761



Internal ID22687977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73674104..73674867hg38UCSC Ensembl
chr8:74586339..74587102hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448365
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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