A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037296



Internal ID19126515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88702791..88809397hg38UCSC Ensembl
Innerchr13:89355045..89461651hg19UCSC Ensembl
Innerchr13:88153046..88259652hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38106607
hg19106607
hg18106607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525453
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)nsv1037296
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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