A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872070



Internal ID22647008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70375891..70381007hg38UCSC Ensembl
chr18:68043127..68048243hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg385117
hg195117
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv976n209
Supporting Variantsnssv17472029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872070
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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