A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451939



Internal ID18274019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86965868..87291715hg38UCSC Ensembl
Innerchr10:88725625..89051472hg19UCSC Ensembl
Innerchr10:88715605..89041452hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38325848
hg19325848
hg18325848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428236
Supporting Variants
SamplesHGDP01086
Known GenesADIRF, AGAP11, FAM25A, FAM35A, GLUD1, NUTM2A, NUTM2A-AS1
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)nssv451939
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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