A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765976



Internal ID18967989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33382101..33396102hg38UCSC Ensembl
chr9:33382099..33396100hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3814002
hg1914002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078056
Supporting Variants
SamplesKWP1
Known GenesAQP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765976
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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