A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132581



Internal ID19260096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:198173829..198185729hg38UCSC Ensembl
Outerchr3:197900700..197912600hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3811901
hg1911901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987365
SamplesKWS1
Known GenesFAM157A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132581
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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