A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849390



Internal ID22624325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36217419..36220871hg38UCSC Ensembl
chr8:36074937..36078389hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383453
hg193453
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2004n209
Supporting Variantsnssv17506005, nssv17506006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849390
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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