A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896731



Internal ID6303742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1713618..2037163hg19UCSC Ensembl
Outerchr11:1709656..2040997hg19UCSC Ensembl
Innerchr11:1670194..1993739hg18UCSC Ensembl
Outerchr11:1666232..1997573hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585932
SamplesIS37646
Known GenesCTSD, H19, IFITM10, KRTAP5-6, LSP1, MIR4298, MIR675, MOB2, MRPL23, MRPL23-AS1, SYT8, TNNI2, TNNT3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896731
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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