A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199533



Internal ID21338329
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3942233
Supporting Variants
SamplesHG002
Known GenesSLC27A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199533
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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