A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1848958



Internal ID17481451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49910159..49929304hg38UCSC Ensembl
Innerchr10:51118205..51137410hg19UCSC Ensembl
Innerchr10:50788211..50807522hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3819146
hg1919206
hg1819312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv947986
Supporting Variants
SamplesHGDP00998
Known GenesPARG
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1848958
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