A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758643



Internal ID17418416
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv983207
Supporting Variants
SamplesHGDP00542
Known GenesPOLD3
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758643
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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