A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851161



Internal ID22626096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66887162..66893303hg38UCSC Ensembl
chr9:40799538..40805679hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386142
hg196142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514059, nssv17514057, nssv17514058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851161
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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