A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037246



Internal ID19126465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55488016..55626808hg38UCSC Ensembl
Innerchr13:56062151..56200943hg19UCSC Ensembl
Innerchr13:54960152..55098944hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38138793
hg19138793
hg18138793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3714989
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)nsv1037246
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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