A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954651



Internal ID17303524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6657095..6657364hg38UCSC Ensembl
Outerchr19:6657106..6657375hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002905
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954651
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