A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952262



Internal ID16954449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104080064..104120863hg38UCSC Ensembl
Outerchr14:104546401..104587200hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3840800
hg1940800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998422
SamplesBILGI_BIOE
Known GenesASPG, MIR203, MIR3545
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952262
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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