A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006890



Internal ID19096108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103759327..103797475hg38UCSC Ensembl
Innerchr3:103478171..103516319hg19UCSC Ensembl
Innerchr3:104960861..104999009hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3838149
hg1938149
hg1838149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604381
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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