A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144284



Internal ID18914789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:99104918..99105518hg38UCSC Ensembl
Outerchr9:101867200..101867800hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995019
SamplesKWS1
Known GenesTGFBR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144284
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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