A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996932



Internal ID16943198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93453119..93478818hg38UCSC Ensembl
Outerchr9:96215401..96241100hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3825700
hg1925700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950899
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM120A, FAM120AOS
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996932
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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