A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909216



Internal ID22684426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74543451..74550195hg38UCSC Ensembl
chr8:75455686..75462430hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386745
hg196745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436648
Samples
Known GenesMIR5681A, MIR5681B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909216
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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