A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949862



Internal ID17298736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:143024364..143028563hg38UCSC Ensembl
Outerchr6:143345501..143349700hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997528
SamplesBILGI_BIOE
Known GenesLOC100507489
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949862
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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