A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998385



Internal ID16944651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:88002357..88011456hg38UCSC Ensembl
Outerchr14:88468701..88477800hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952879
Supporting Variants
SamplesBILGI_BIOE
Known GenesGPR65
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998385
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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