A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944951



Internal ID22720423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88646389..88660731hg38UCSC Ensembl
chr15:89189620..89203962hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3814343
hg1914343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384174
Samples
Known GenesISG20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944951
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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