A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110564



Internal ID19261066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40929944..41047292hg38UCSC Ensembl
Outerchr9:68664200..68781600hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38117349
hg19117401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960218
SamplesKWS1
Known GenesLOC100132352
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110564
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