A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855133



Internal ID22630068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64036512..64046617hg38UCSC Ensembl
chrUn_gl000211:68065..78170hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810106
hg1910106
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2132n209
Supporting Variantsnssv17513940, nssv17513939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855133
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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