A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509692



Internal ID20883003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95323101..95330600hg38UCSC Ensembl
chr15:95866330..95873829hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183199
Samples
Known GenesLOC400456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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