A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977230



Internal ID18612436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41384062..41385025hg38UCSC Ensembl
Innerchr13:41958198..41959161hg19UCSC Ensembl
Innerchr13:40856198..40857161hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38964
hg19964
hg18964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1962053, nssv1962052, nssv1962048, nssv1962054, nssv1962046, nssv1962055, nssv1962051, nssv1962050, nssv1962049, nssv1962047
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977230
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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