A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044533



Internal ID19133752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34425976..34456603hg38UCSC Ensembl
Innerchr13:35000113..35030740hg19UCSC Ensembl
Innerchr13:33898113..33928740hg18UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3830628
hg1930628
hg1830628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523243
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)nsv1044533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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