A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983972



Internal ID18619163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105505131..105568591hg38UCSC Ensembl
Innerchr14:105971468..106034928hg19UCSC Ensembl
Innerchr14:105042513..105105973hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3863461
hg1963461
hg1863461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763235
SamplesHGDP00998
Known GenesTMEM121
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983972
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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