A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514617



Internal ID20887972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89285801..89287200hg38UCSC Ensembl
chr15:89829032..89830431hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026876
Samples
Known GenesFANCI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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