A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829089



Internal ID15776359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70484517..70545017hg38UCSC Ensembl
Innerchr14:70951234..71011734hg19UCSC Ensembl
Innerchr14:70020987..70081487hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3860501
hg1960501
hg1860501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565042
Supporting Variants
Samples
Known GenesADAM20
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829089
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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