A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148633



Internal ID15855406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105124547..105167162hg38UCSC Ensembl
Innerchr14:105590884..105633499hg19UCSC Ensembl
Innerchr14:104661929..104704544hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3842616
hg1942616
hg1842616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566154
Supporting Variants
Samples1780862585_A
Known GenesJAG2, MIR6765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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