A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146502



Internal ID18854684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123177..69128442hg38UCSC Ensembl
Outerchr9:71738093..71743358hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385266
hg195266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995655
SamplesKWB1
Known GenesTJP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146502
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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