A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942233



Internal ID21362302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128356700..128356850hg38UCSC Ensembl
chr9:131118979..131119129hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199533
SamplesHG002
Known GenesSLC27A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942233
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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