A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132728



Internal ID19259640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64396082..64403482hg38UCSC Ensembl
Outerchr9:69408500..69415900hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg387401
hg197401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987518
SamplesKWS1
Known GenesANKRD20A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132728
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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