A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1765436



Internal ID17531398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26426339..26429437hg38UCSC Ensembl
Innerchr1:26752830..26755928hg19UCSC Ensembl
Innerchr1:26625417..26628515hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383099
hg193099
hg183099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945840
Supporting Variants
SamplesHGDP01307
Known GenesLIN28A
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)nssv1765436
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