A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998362



Internal ID16944628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:68788584..68795783hg38UCSC Ensembl
Outerchr14:69255301..69262500hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952859
Supporting Variants
SamplesBILGI_BIOE
Known GenesZFP36L1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998362
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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