A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956318



Internal ID16958506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:98892940..98895632hg38UCSC Ensembl
Outerchr4:99814091..99816783hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382693
hg192693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004712
SamplesBILGI_BIOE
Known GenesEIF4E
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956318
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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