A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949826



Internal ID17298700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:140639947..140645746hg38UCSC Ensembl
Outerchr4:141561101..141566900hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996786
SamplesBILGI_BIOE
Known GenesTBC1D9, TNRC18P1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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