A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1867982



Internal ID17870382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110547193..110550290hg38UCSC Ensembl
Innerchr10:112306951..112310048hg19UCSC Ensembl
Innerchr10:112296941..112300038hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383098
hg193098
hg183098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948184
Supporting Variants
SamplesHGDP01284
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)nssv1867982
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