A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952036



Internal ID17300910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:57561989..57582388hg38UCSC Ensembl
Outerchr16:57595901..57616300hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3820400
hg1920400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000153
SamplesBILGI_BIOE
Known GenesGPR114
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952036
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