A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1877471



Internal ID17812998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18403305..18409759hg38UCSC Ensembl
Innerchr11:18424852..18431306hg19UCSC Ensembl
Innerchr11:18381428..18387882hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386455
hg196455
hg186455
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982991
Supporting Variants
SamplesHGDP00927
Known GenesLDHA
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1877471
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