A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv451944



Internal ID18274873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86965868..87445609hg38UCSC Ensembl
Innerchr10:88725625..89205366hg19UCSC Ensembl
Innerchr10:88715605..89195346hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38479742
hg19479742
hg18479742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv428236
Supporting Variants
SamplesNA19113
Known GenesADIRF, AGAP11, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
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)nssv451944
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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