A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151719



Internal ID19202810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67882553..67885854hg38UCSC Ensembl
Outerchr9:67949999..67953300hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg383302
hg193302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003146
SamplesKWB1
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151719
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