A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042200



Internal ID19131419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101618261..101714058hg38UCSC Ensembl
Innerchr15:102158464..102254261hg19UCSC Ensembl
Innerchr15:99975987..100071784hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3895798
hg1995798
hg1895798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2680n100
Supporting Variantsnssv3718230, nssv3555388, nssv3555389, nssv3555391, nssv3555384, nssv3555387, nssv3718231, nssv3555385, nssv3555386, nssv3555390
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042200
Frequency
Sample Size11257
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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