A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035645



Internal ID19124864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:30833939..30864668hg38UCSC Ensembl
Innerchr13:31408076..31438805hg19UCSC Ensembl
Innerchr13:30306076..30336805hg18UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3830730
hg1930730
hg1830730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1624n100
Supporting Variantsnssv3523221
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)nsv1035645
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