A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856643



Internal ID22631578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42943259..42951668hg38UCSC Ensembl
chr9:44019451..44027860hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388410
hg198410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2118n209
Supporting Variantsnssv17513521, nssv17513522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856643
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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