A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1832677



Internal ID17777776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21101856..21113598hg38UCSC Ensembl
Innerchr10:21390785..21402527hg19UCSC Ensembl
Innerchr10:21430791..21442533hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3811743
hg1911743
hg1811743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947764
Supporting Variants
SamplesHGDP00665
Known GenesNEBL
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)nssv1832677
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