A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515487



Internal ID20888847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94752974..94756509hg38UCSC Ensembl
chr15:95296203..95299738hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg383536
hg193536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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