A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870617



Internal ID22645553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63512712..63523592hg38UCSC Ensembl
chr18:61179945..61190825hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3810881
hg1910881
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870617
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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