A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041501



Internal ID18784032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:50109053..50221059hg38UCSC Ensembl
Innerchr13:50683189..50795195hg19UCSC Ensembl
Innerchr13:49581190..49693196hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38112007
hg19112007
hg18112007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523458
Samples
Known GenesDLEU2, ST13P4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041501
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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