A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864148



Internal ID22639083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68264147..68281371hg38UCSC Ensembl
chr15:68556485..68573709hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3817225
hg1917225
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473556
Samples
Known GenesFEM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864148
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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