A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514264



Internal ID20887616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36185549..36261280hg38UCSC Ensembl
chr15:36477750..36553481hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3875732
hg1975732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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