A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1766705



Internal ID17448777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25887321..25891977hg38UCSC Ensembl
Innerchr1:26213812..26218468hg19UCSC Ensembl
Innerchr1:26086399..26091055hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384657
hg194657
hg184657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945838
Supporting Variants
SamplesHGDP00778
Known GenesSTMN1
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)nssv1766705
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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