A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866334



Internal ID22641269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86128284..86156729hg38UCSC Ensembl
chr8:87140513..87168958hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3828446
hg1928446
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510145
Samples
Known GenesATP6V0D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866334
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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