A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135288



Internal ID18940198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69189630..69190077hg38UCSC Ensembl
Outerchr9:71804546..71804993hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4065n106
Supporting Variantsnssv3988846
SamplesKWS2
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135288
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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