A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428455



Internal ID18278219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167727908..168130542hg38UCSC Ensembl
Innerchr4:168649059..169051693hg19UCSC Ensembl
Innerchr4:168885634..169288268hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38402635
hg19402635
hg18402635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450208, nssv450190, nssv450188, nssv450207, nssv450200, nssv450194, nssv450203, nssv450189, nssv450184, nssv450206, nssv450192, nssv450202, nssv450196, nssv450180, nssv450183, nssv450191, nssv450182, nssv450178, nssv450197, nssv450210, nssv450201, nssv450186, nssv450179, nssv450205, nssv450193, nssv450199, nssv450181, nssv450195, nssv450185, nssv450204
SamplesHGDP00450, HGDP00474, HGDP00463, HGDP00984, NA19257, NA19108, NA19147, HGDP00476, HGDP00462, HGDP01093, HGDP01087, HGDP01094, NA19096, NA18916, NA19181, HGDP01089, NA19189, HGDP00467, NA18498, HGDP00986, HGDP01088, HGDP01086, NA19225, HGDP00478, NA19113, HGDP00460, HGDP00473, HGDP00449, HGDP00472, HGDP00471
Known GenesANXA10
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)nsv428455
Frequency
Sample Size62
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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