A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952257



Internal ID16954444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:103067564..103135963hg38UCSC Ensembl
Outerchr14:103533901..103602300hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3868400
hg1968400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998417
SamplesBILGI_BIOE
Known GenesEXOC3L4, TNFAIP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952257
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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