A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075663



Internal ID18970158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93451517..93451918hg38UCSC Ensembl
chr9:96213799..96214200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772276
SamplesKWP1
Known GenesFAM120A, FAM120AOS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075663
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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