A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851769



Internal ID22626704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40656237..40666303hg38UCSC Ensembl
chr15:40948435..40958501hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810067
hg1910067
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471812
Samples
Known GenesCASC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851769
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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