A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043434



Internal ID19132653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84981838..85054662hg38UCSC Ensembl
Innerchr13:85555973..85628797hg19UCSC Ensembl
Innerchr13:84453974..84526798hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3872825
hg1972825
hg1872825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713254
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)nsv1043434
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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