A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077132



Internal ID19321060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66704393..66706394hg38UCSC Ensembl
chr9:66041799..66043800hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg382002
hg192002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770251
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077132
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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