A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075667



Internal ID18970897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103013217..103014218hg38UCSC Ensembl
chr9:105775499..105776500hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767601
SamplesKWP1
Known GenesCYLC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075667
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer