A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119196



Internal ID19274974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:35605303..35605603hg38UCSC Ensembl
Outerchr9:35605300..35605600hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982002
SamplesKWS1
Known GenesTESK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119196
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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