A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv58



Internal ID15383816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:128462151..128467177hg38UCSC Ensembl
Outerchr10:130260415..130265441hg19UCSC Ensembl
Outerchr10:130150405..130155431hg18UCSC Ensembl
Outerchr10:130150405..130155431hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3811796
hg1911796
hg1811796
hg1711796
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv58
SamplesNA15510
Known Genes
MethodSequencing
AnalysisFosmids were categorized as discordant if the in silico size was in excess of three standard deviations from the mean (<32 or 48> kb) and/or showed incorrect orientation of ends
PlatformCapillary
Comments
ReferenceTuzun_et_al_2005
Pubmed ID15895083
Accession Number(s)nsv58
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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