A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035427



Internal ID19124646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85965713..86013952hg38UCSC Ensembl
Innerchr13:86539848..86588087hg19UCSC Ensembl
Innerchr13:85437849..85486088hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3848240
hg1948240
hg1848240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525421
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)nsv1035427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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