A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849014



Internal ID22623949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64751204..64756078hg38UCSC Ensembl
chr15:65043403..65048277hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384875
hg194875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473530
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849014
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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