A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129755



Internal ID18919672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:180615336..180615497hg38UCSC Ensembl
Outerchr5:180042336..180042497hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964082
SamplesKWS1
Known GenesFLT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129755
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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