A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956232



Internal ID17305105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34889395..34889497hg38UCSC Ensembl
Outerchr20:33477198..33477300hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003207
SamplesBILGI_BIOE
Known GenesACSS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956232
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