A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950617



Internal ID16952804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:370186..375385hg38UCSC Ensembl
Outerchr5:370301..375500hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997676
SamplesBILGI_BIOE
Known GenesAHRR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950617
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