A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2541238



Internal ID17434393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61862957..61910760hg38UCSC Ensembl
Innerchr9:44999109..45046912hg19UCSC Ensembl
Innerchr9:44939105..44986908hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3847804
hg1947804
hg1847804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982258
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2541238
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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