A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040200



Internal ID19129419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70167253..70204707hg38UCSC Ensembl
Innerchr13:70741385..70778839hg19UCSC Ensembl
Innerchr13:69639386..69676840hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3837455
hg1937455
hg1837455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1712n100
Supporting Variantsnssv3713231
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)nsv1040200
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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