A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863774



Internal ID22638709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36217620..36221471hg38UCSC Ensembl
chr8:36075138..36078989hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383852
hg193852
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2004n209
Supporting Variantsnssv17506009, nssv17506010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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