A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511212



Internal ID20884538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71305819..71436019hg38UCSC Ensembl
chr15:71598158..71728358hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38130201
hg19130201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026384
Samples
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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