A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955651



Internal ID17304524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166755894..166761909hg38UCSC Ensembl
Outerchr4:167677045..167683060hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000616
SamplesBILGI_BIOE
Known GenesSPOCK3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955651
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer