A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955806



Internal ID17304679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:19483031..19496286hg38UCSC Ensembl
Outerchr6:19483262..19496517hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813256
hg1913256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003380
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955806
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