A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1868209



Internal ID17796011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116748475..116752294hg38UCSC Ensembl
Innerchr10:118507986..118511805hg19UCSC Ensembl
Innerchr10:118497976..118501795hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383820
hg193820
hg183820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948196
Supporting Variants
SamplesHGDP00778
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)nssv1868209
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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