A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051533



Internal ID19140752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34352755..34443149hg38UCSC Ensembl
Innerchr13:34926892..35017286hg19UCSC Ensembl
Innerchr13:33824892..33915286hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3890395
hg1990395
hg1890395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523242
Samples
Known GenesLINC00457
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051533
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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