A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852961



Internal ID22627896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49580125..49594564hg38UCSC Ensembl
chr15:49872322..49886761hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3814440
hg1914440
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471948
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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