A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046278



Internal ID19135497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86808989..87059976hg38UCSC Ensembl
Innerchr13:87461244..87712231hg19UCSC Ensembl
Innerchr13:86259245..86510232hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38250988
hg19250988
hg18250988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1723n100
Supporting Variantsnssv3525439
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)nsv1046278
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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