A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996909



Internal ID17289861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81707486..81713085hg38UCSC Ensembl
Outerchr9:84322401..84328000hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950874
Supporting Variants
SamplesBILGI_BIOE
Known GenesLOC101927502
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996909
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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