A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117528



Internal ID19263403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132378456..132378622hg38UCSC Ensembl
Outerchr9:135253843..135254009hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980108
SamplesKWS2
Known GenesTTF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117528
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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