A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038055



Internal ID19127274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26806677..26837226hg38UCSC Ensembl
Innerchr13:27380814..27411363hg19UCSC Ensembl
Innerchr13:26278814..26309363hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3830550
hg1930550
hg1830550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1623n100
Supporting Variantsnssv3714958
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)nsv1038055
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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