A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950332



Internal ID16952519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:1364213..1367912hg38UCSC Ensembl
Outerchr4:1358001..1361700hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996621
SamplesBILGI_BIOE
Known GenesUVSSA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950332
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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