A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624958



Internal ID15848494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:96707122..96709686hg38UCSC Ensembl
Outerchr14:97173459..97176023hg19UCSC Ensembl
Outerchr14:96243212..96245776hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382565
hg192565
hg182565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512371
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624958
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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