A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952826



Internal ID16955013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:36653796..36663795hg38UCSC Ensembl
Outerchr14:37123001..37133000hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998326
SamplesBILGI_BIOE
Known GenesPAX9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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