A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986892



Internal ID19222062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:140349343..140349395hg38UCSC Ensembl
Outerchr8:141359442..141359494hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124384
Supporting Variants
SamplesKWS1
Known GenesTRAPPC9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986892
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