A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1897444



Internal ID17432352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77917029..77960334hg38UCSC Ensembl
Innerchr11:77628075..77671380hg19UCSC Ensembl
Innerchr11:77305723..77349028hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843306
hg1943306
hg1843306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv975205
Supporting Variants
SamplesHGDP00665
Known GenesINTS4
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)nssv1897444
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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