A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957175



Internal ID16959362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14326749..14327087hg38UCSC Ensembl
Outerchr11:14348295..14348633hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004992
SamplesBILGI_BIOE
Known GenesRRAS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957175
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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