A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135143



Internal ID19273100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81858347..81858681hg38UCSC Ensembl
Outerchr3:81907498..81907832hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2553n106
Supporting Variantsnssv3988695
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135143
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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