A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1877520



Internal ID17417339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11352691..11353287hg38UCSC Ensembl
Innerchr11:11374238..11374834hg19UCSC Ensembl
Innerchr11:11330814..11331410hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv975884
Supporting Variants
SamplesHGDP00542
Known GenesCSNK2A3, GALNT18
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1877520
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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