A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949866



Internal ID17298740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:149317065..149318664hg38UCSC Ensembl
Outerchr6:149638201..149639800hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997532
SamplesBILGI_BIOE
Known GenesTAB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949866
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