A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006673



Internal ID22068304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96898097..96927058hg38UCSC Ensembl
Outerchr9:96896925..96943417hg38UCSC Ensembl
Innerchr9:99660379..99689340hg19UCSC Ensembl
Outerchr9:99659207..99705699hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3846493
hg1946493
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154520
Supporting Variants
Samples
Known GenesLOC441454, NUTM2G
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006673
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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