A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115209



Internal ID18915261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92511371..92511428hg38UCSC Ensembl
Outerchr9:95273653..95273710hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976263
SamplesKWS2
Known GenesCENPP, ECM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115209
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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