A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051182



Internal ID18793713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96808751..96870702hg38UCSC Ensembl
Innerchr14:97275088..97337039hg19UCSC Ensembl
Innerchr14:96344841..96406792hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3861952
hg1961952
hg1861952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532635
Samples
Known GenesVRK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051182
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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