A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451814



Internal ID18621264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38363073..38529907hg38UCSC Ensembl
Innerchr10:38652001..38818835hg19UCSC Ensembl
Innerchr10:38692007..38858841hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38166835
hg19166835
hg18166835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428230
Supporting Variants
SamplesNA18916
Known GenesHSD17B7P2, LINC00999, SEPT7P9
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)nssv451814
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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