A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915847



Internal ID22691065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28682626..28682901hg38UCSC Ensembl
chr10:28971555..28971830hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368181
Samples
Known GenesBAMBI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915847
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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