A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847567



Internal ID22622502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81635142..81651196hg38UCSC Ensembl
chr15:81927483..81943537hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3816055
hg1916055
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv761n209
Supporting Variantsnssv17474240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847567
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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