A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053818



Internal ID19143037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:38938137..38958874hg38UCSC Ensembl
Innerchr13:39512274..39533011hg19UCSC Ensembl
Innerchr13:38410274..38431011hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3820738
hg1920738
hg1820738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523380
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)nsv1053818
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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