A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952279



Internal ID16954466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105136864..105237863hg38UCSC Ensembl
Outerchr14:105603201..105704200hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38101000
hg19101000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998439
SamplesBILGI_BIOE
Known GenesBRF1, JAG2, MIR6765, NUDT14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952279
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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