A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999369



Internal ID16945635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14313402..14315801hg38UCSC Ensembl
Outerchr9:14313401..14315800hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950837
Supporting Variants
SamplesBILGI_BIOE
Known GenesNFIB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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