A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951270



Internal ID16953457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:528401..628100hg38UCSC Ensembl
Outerchr11:528401..628100hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899700
hg1999700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998112
SamplesBILGI_BIOE
Known GenesC11orf35, CDHR5, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, SCT
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951270
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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