A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983207



Internal ID18271715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:74630040..74633321hg38UCSC Ensembl
Innerchr11:74341085..74344366hg19UCSC Ensembl
Innerchr11:74018733..74022014hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383282
hg193282
hg183282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758643
SamplesHGDP00542
Known GenesPOLD3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983207
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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