A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591195



Internal ID16378604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103378433..103460844hg38UCSC Ensembl
Innerchr3:103097277..103179688hg19UCSC Ensembl
Innerchr3:104579967..104662378hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3882412
hg1982412
hg1882412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8485n54
Supporting Variantsnssv1152508
Samples1780854599_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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