A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1833218



Internal ID17777798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15170248..15172688hg38UCSC Ensembl
Innerchr10:15212247..15214687hg19UCSC Ensembl
Innerchr10:15252253..15254693hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382441
hg192441
hg182441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947749
Supporting Variants
SamplesHGDP00665
Known Genes
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)nssv1833218
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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