A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv65



Internal ID15383824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5760863..5791003hg38UCSC Ensembl
Outerchr11:5782093..5812233hg19UCSC Ensembl
Outerchr11:5738669..5768809hg18UCSC Ensembl
Outerchr11:5738669..5768809hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3830141
hg1930141
hg1830141
hg1730141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv65
SamplesNA15510
Known GenesOR52N1, OR52N5
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)nsv65
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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