A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768276



Internal ID19310916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128130520..128138321hg38UCSC Ensembl
chr9:130892799..130900600hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg387802
hg197802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078654
Supporting Variants
SamplesKWP1
Known GenesPTGES2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768276
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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