A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955578



Internal ID16957765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:159711194..159711405hg38UCSC Ensembl
Outerchr3:159428983..159429194hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004575
SamplesBILGI_BIOE
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955578
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