A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1835461



Internal ID17877106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19919501..19921377hg38UCSC Ensembl
Innerchr10:20208430..20210306hg19UCSC Ensembl
Innerchr10:20248436..20250312hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381877
hg191877
hg181877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947762
Supporting Variants
SamplesHGDP01307
Known GenesPLXDC2
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)nssv1835461
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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