A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451765



Internal ID18620583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107694332..107870043hg38UCSC Ensembl
Innerchr9:110456613..110632324hg19UCSC Ensembl
Innerchr9:109496434..109672145hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38175712
hg19175712
hg18175712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428221
Supporting Variants
SamplesHGDP00984
Known Genes
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nssv451765
Frequency
Sample Size62
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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