A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950331



Internal ID16952518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1164113..1239212hg38UCSC Ensembl
Outerchr4:1157901..1233000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3875100
hg1975100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996620
SamplesBILGI_BIOE
Known GenesCTBP1, CTBP1-AS, LOC100130872, SPON2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950331
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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