A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1753699



Internal ID17876868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:269665..297968hg38UCSC Ensembl
Innerchr1:239416..267719hg19UCSC Ensembl
Innerchr1:229279..257704hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3828304
hg1928304
hg1828426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv945709
Supporting Variants
SamplesHGDP01307
Known Genes
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)nssv1753699
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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