A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7697



Internal ID15552732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:18906234..18960343hg38UCSC Ensembl
Outerchr11:18927781..18981890hg19UCSC Ensembl
Outerchr11:18884357..18938466hg18UCSC Ensembl
Outerchr11:18884357..18938466hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3854110
hg1954110
hg1854110
hg1754110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10806
SamplesNA18956
Known GenesMRGPRX1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7697
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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