A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109841



Internal ID18907229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123182..69128489hg38UCSC Ensembl
Outerchr9:71738098..71743405hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385308
hg195308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4064n106
Supporting Variantsnssv3958232
SamplesKWS1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109841
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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