A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428184



Internal ID18277948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:114211558..114385441hg38UCSC Ensembl
Innerchr7:113851613..114025496hg19UCSC Ensembl
Innerchr7:113638849..113812732hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38173884
hg19173884
hg18173884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451244
SamplesHGDP00473
Known GenesFOXP2
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)nsv428184
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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