A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848219



Internal ID22623154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42473706..42495579hg38UCSC Ensembl
chr9:44475540..44497413hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821874
hg1921874
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2115n209
Supporting Variantsnssv17513429, nssv17513430, nssv17513428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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