A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950574



Internal ID16952761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38663380..38665179hg38UCSC Ensembl
Outerchr4:38665001..38666800hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996700
SamplesBILGI_BIOE
Known GenesFLJ13197, KLF3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950574
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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