A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950336



Internal ID17299210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1486576..1521273hg38UCSC Ensembl
Outerchr4:1488301..1523000hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834698
hg1934700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996624
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950336
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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