A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129704



Internal ID19282204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:177457361..177457419hg38UCSC Ensembl
Outerchr3:177175149..177175207hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964010
SamplesKWS1
Known GenesLINC00578
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129704
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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