A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949891



Internal ID17298765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166898213..166908412hg38UCSC Ensembl
Outerchr6:167311701..167321900hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810200
hg1910200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997557
SamplesBILGI_BIOE
Known GenesRPS6KA2-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949891
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