A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1765340



Internal ID17745770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26126760..26129641hg38UCSC Ensembl
Innerchr1:26453251..26456132hg19UCSC Ensembl
Innerchr1:26325838..26328719hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382882
hg192882
hg182882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945839
Supporting Variants
SamplesHGDP00521
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)nssv1765340
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