A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428160



Internal ID18624610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6897318..7179922hg38UCSC Ensembl
Innerchr7:6936949..7219553hg19UCSC Ensembl
Innerchr7:6903474..7186078hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38282605
hg19282605
hg18282605
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450917, nssv450918
SamplesHGDP00462, NA19113
Known GenesLOC100131257
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)nsv428160
Frequency
Sample Size62
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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