A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451965



Internal ID18620898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113894004..114008148hg38UCSC Ensembl
Innerchr10:115653763..115767907hg19UCSC Ensembl
Innerchr10:115643753..115757897hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38114145
hg19114145
hg18114145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428238
Supporting Variants
SamplesHGDP01089
Known GenesNHLRC2
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)nssv451965
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