A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949829



Internal ID16952016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:150078249..150079948hg38UCSC Ensembl
Outerchr4:150999401..151001100hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996789
SamplesBILGI_BIOE
Known GenesDCLK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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