A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035356



Internal ID19124575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103602304..103930807hg38UCSC Ensembl
Innerchr13:104254654..104583157hg19UCSC Ensembl
Innerchr13:103052655..103381158hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38328504
hg19328504
hg18328504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525546, nssv3525547
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)nsv1035356
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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