A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041208



Internal ID19130427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37502118..37539478hg38UCSC Ensembl
Innerchr13:38076255..38113615hg19UCSC Ensembl
Innerchr13:36974255..37011615hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3837361
hg1937361
hg1837361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1628n100
Supporting Variantsnssv3523314
Samples
Known GenesLINC00547
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041208
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