A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950138



Internal ID17299012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:21361170..21367169hg38UCSC Ensembl
Outerchr6:21361401..21367400hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997410
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950138
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