A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498617



Internal ID20871829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52647801..52649800hg38UCSC Ensembl
chr15:52939998..52941997hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024078
Samples
Known GenesFAM214A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498617
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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