A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872268



Internal ID22647207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59687637..59717306hg38UCSC Ensembl
chr18:57354869..57384538hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3829670
hg1929670
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471382
Samples
Known GenesCCBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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