A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054497



Internal ID19143716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103602304..103625669hg38UCSC Ensembl
Innerchr13:104254654..104278019hg19UCSC Ensembl
Innerchr13:103052655..103076020hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3823366
hg1923366
hg1823366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1735n100
Supporting Variantsnssv3713293
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)nsv1054497
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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