A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055031



Internal ID19144250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58257879..58300635hg38UCSC Ensembl
Innerchr13:58832013..58874769hg19UCSC Ensembl
Innerchr13:57730014..57772770hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3842757
hg1942757
hg1842757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526582, nssv3526581
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)nsv1055031
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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