A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv71



Internal ID15037154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55591549..55702883hg38UCSC Ensembl
Outerchr11:55359025..55470359hg19UCSC Ensembl
Outerchr11:55115601..55226935hg18UCSC Ensembl
Outerchr11:55115601..55226935hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38111335
hg19111335
hg18111335
hg17111335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv71
SamplesNA15510
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
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)nsv71
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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