A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955148



Internal ID17304021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62064645..62066444hg38UCSC Ensembl
Outerchr20:60639701..60641500hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000010
SamplesBILGI_BIOE
Known GenesTAF4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955148
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