A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953589



Internal ID16955776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:46601544..46636643hg38UCSC Ensembl
Outerchr19:47104801..47139900hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3835100
hg1935100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999855
SamplesBILGI_BIOE
Known GenesCALM3, GNG8, PTGIR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953589
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