A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428151



Internal ID18277915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100006066..100166527hg38UCSC Ensembl
Innerchr6:100453942..100614403hg19UCSC Ensembl
Innerchr6:100560663..100721124hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38160462
hg19160462
hg18160462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv450826
SamplesNA19096
Known GenesMCHR2-AS1
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)nsv428151
Frequency
Sample Size62
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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