A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1867883



Internal ID17795999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110448221..110455403hg38UCSC Ensembl
Innerchr10:112207979..112215161hg19UCSC Ensembl
Innerchr10:112197969..112205151hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg387183
hg197183
hg187183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948183
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)nssv1867883
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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