A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957996



Internal ID18861346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:80492676..80492738hg38UCSC Ensembl
Outerchr8:81404911..81404973hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1117835
Supporting Variants
SamplesKWS1
Known GenesZBTB10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957996
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