A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv110



Internal ID15036901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34393029..34548563hg38UCSC Ensembl
Outerchr15:34685230..34840764hg19UCSC Ensembl
Outerchr15:32472522..32628056hg18UCSC Ensembl
Outerchr15:32472522..32628056hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38155535
hg19155535
hg18155535
hg17155535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv110
SamplesNA15510
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
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)nsv110
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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