A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077560



Internal ID19322553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90216517..90223818hg38UCSC Ensembl
chr9:92978799..92986100hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg387302
hg197302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763696
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077560
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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