A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045646



Internal ID19134865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81543374..81570856hg38UCSC Ensembl
Innerchr13:82117509..82144991hg19UCSC Ensembl
Innerchr13:81015510..81042992hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3827483
hg1927483
hg1827483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713243
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)nsv1045646
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer