A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012513



Internal ID19101730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:115433791..115463856hg38UCSC Ensembl
Innerchr3:115152638..115182703hg19UCSC Ensembl
Innerchr3:116635328..116665393hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3830066
hg1930066
hg1830066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604469
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)nsv1012513
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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