A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998152



Internal ID16944418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:13961154..13964653hg38UCSC Ensembl
Outerchr11:13982701..13986200hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951310
Supporting Variants
SamplesBILGI_BIOE
Known GenesSPON1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998152
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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