A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348930



Internal ID22267503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93027451..93028700hg38UCSC Ensembl
chr9:95789733..95790982hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218549
Supporting Variants
SamplesNA19238
Known GenesFGD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348930
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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