A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955342



Internal ID16957529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:127666758..127678357hg38UCSC Ensembl
Outerchr3:127385601..127397200hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001459
SamplesBILGI_BIOE
Known GenesABTB1, PODXL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955342
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