A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501753



Internal ID20874990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45198600..45200407hg38UCSC Ensembl
chr15:45490798..45492605hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381808
hg191808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189682
Samples
Known GenesSHF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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