A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952819



Internal ID16955006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:24367695..24377694hg38UCSC Ensembl
Outerchr14:24836901..24846900hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998318
SamplesBILGI_BIOE
Known GenesNFATC4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952819
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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