A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044558



Internal ID19133777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86409582..86448695hg38UCSC Ensembl
Innerchr13:87061837..87100950hg19UCSC Ensembl
Innerchr13:85859838..85898951hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3839114
hg1939114
hg1839114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525427
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)nsv1044558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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