A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037473



Internal ID19126692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87108636..87152908hg38UCSC Ensembl
Innerchr13:87760891..87805163hg19UCSC Ensembl
Innerchr13:86558892..86603164hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3844273
hg1944273
hg1844273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525442
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)nsv1037473
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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