A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999482



Internal ID17292434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62383800..62447899hg38UCSC Ensembl
Outerchr9:46695101..46759200hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3864100
hg1964100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951173
Supporting Variants
SamplesBILGI_BIOE
Known GenesKGFLP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999482
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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