A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066190



Internal ID18808721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36339397..36361975hg38UCSC Ensembl
Innerchr19:36830299..36852877hg19UCSC Ensembl
Innerchr19:41522139..41544717hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3822579
hg1922579
hg1822579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568182
Samples
Known GenesZFP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066190
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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