A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051097



Internal ID19140316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18471488..18683428hg38UCSC Ensembl
Innerchr13:19045628..19257568hg19UCSC Ensembl
Innerchr13:17943628..18155568hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38211941
hg19211941
hg18211941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1599n100
Supporting Variantsnssv3526411, nssv3526412, nssv3526413
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)nsv1051097
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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