A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134906



Internal ID19278287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155733437..155733494hg38UCSC Ensembl
Outerchr7:155526131..155526188hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988397
SamplesKWS1
Known GenesRBM33
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134906
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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