A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999635



Internal ID16945901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:124744805..124748804hg38UCSC Ensembl
Outerchr11:124614701..124618700hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952751
Supporting Variants
SamplesBILGI_BIOE
Known GenesNRGN, VSIG2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999635
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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