A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428210



Internal ID18624660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37977890..38154218hg38UCSC Ensembl
Innerchr9:37977887..38154215hg19UCSC Ensembl
Innerchr9:37967887..38144215hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38176329
hg19176329
hg18176329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv451657, nssv451665, nssv451658, nssv451663, nssv451661, nssv451655, nssv451666, nssv451659, nssv451662, nssv451656, nssv451660
SamplesHGDP01088, HGDP01089, NA18916, NA18498, HGDP00476, NA19257, NA19225, HGDP00472, HGDP00474, HGDP00471, HGDP00478
Known GenesSHB
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)nsv428210
Frequency
Sample Size62
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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