A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956066



Internal ID19211567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44047485..44047884hg38UCSC Ensembl
Outerchr20:42676125..42676524hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121237
Supporting Variants
SamplesKWS1
Known GenesTOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956066
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer