A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115217



Internal ID18911467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:105714022..105716661hg38UCSC Ensembl
Outerchr9:108476303..108478942hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382640
hg192640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976272
SamplesKWS2
Known GenesTMEM38B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115217
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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