A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054843



Internal ID19144062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55252232..55782165hg38UCSC Ensembl
Innerchr13:55826367..56356299hg19UCSC Ensembl
Innerchr13:54724368..55254300hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38529934
hg19529933
hg18529933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523863
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)nsv1054843
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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