A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1897261



Internal ID17448541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77867702..77870923hg38UCSC Ensembl
Innerchr11:77578748..77581969hg19UCSC Ensembl
Innerchr11:77256396..77259617hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383222
hg193222
hg183222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975953
Supporting Variants
SamplesHGDP00778
Known GenesAAMDC
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)nssv1897261
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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