A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856554



Internal ID22631489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49916662..49917961hg38UCSC Ensembl
chr13:50490798..50492097hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458379
Samples
Known GenesSPRYD7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856554
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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