A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046460



Internal ID19135679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28183900..28235034hg38UCSC Ensembl
Innerchr13:28758037..28809171hg19UCSC Ensembl
Innerchr13:27656037..27707171hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3851135
hg1951135
hg1851135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523218
Samples
Known GenesPAN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046460
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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