A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996036



Internal ID19192705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65746145..65755046hg38UCSC Ensembl
Outerchr9:70410999..70419900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg388902
hg198902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150561
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996036
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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