A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004938



Internal ID17297890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47036062..47042152hg38UCSC Ensembl
Outerchr11:47057613..47063703hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386091
hg196091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958580
Supporting Variants
SamplesBILGI_BIOE
Known GenesC11orf49
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004938
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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