A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496383



Internal ID20869584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46564042..46811874hg38UCSC Ensembl
chr15:46856240..47104072hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38247833
hg19247833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496383
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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