A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851334



Internal ID22626269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38755120..38771167hg38UCSC Ensembl
chr15:39047321..39063368hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3816048
hg1916048
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv746n209
Supporting Variantsnssv17471626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851334
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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