A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198999



Internal ID21337795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121092516..121092683hg38UCSC Ensembl
chr9:123854794..123854961hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3951255
Supporting Variants
SamplesHG002
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198999
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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