A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510576



Internal ID20883896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37461234..37501904hg38UCSC Ensembl
chr15:37753435..37794105hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3840671
hg1940671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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