A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513890



Internal ID20887239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65354701..65356600hg38UCSC Ensembl
chr15:65647039..65648938hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180988
Samples
Known GenesIGDCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513890
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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