A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039183



Internal ID18781714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27600204..27632386hg38UCSC Ensembl
Innerchr13:28174341..28206523hg19UCSC Ensembl
Innerchr13:27072341..27104523hg18UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3832183
hg1932183
hg1832183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523217
Samples
Known GenesLNX2, POLR1D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039183
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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