A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428166



Internal ID18624616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61073885..61293876hg38UCSC Ensembl
Innerchr7:61056610..61276601hg19UCSC Ensembl
Innerchr7:61060552..61280543hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg38219992
hg19219992
hg18219992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450995, nssv451004, nssv451010, nssv451001, nssv451006, nssv451002, nssv451009, nssv450998, nssv450996, nssv451003, nssv450999, nssv451000, nssv451011, nssv450993, nssv450994, nssv451007, nssv451005
SamplesHGDP01087, HGDP01093, HGDP01088, HGDP00476, HGDP00460, HGDP00450, HGDP00473, HGDP00986, HGDP00467, NA19257, NA19225, HGDP01094, HGDP00472, HGDP00471, HGDP00478, HGDP01086, HGDP00449
Known Genes
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)nsv428166
Frequency
Sample Size62
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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