A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848213



Internal ID22623148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64034872..64046105hg38UCSC Ensembl
chrUn_gl000211:66425..77658hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811234
hg1911234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2132n209
Supporting Variantsnssv17513937, nssv17513938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848213
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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