A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060306



Internal ID18802837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14697771..14721224hg38UCSC Ensembl
Innerchr19:14808583..14832036hg19UCSC Ensembl
Innerchr19:14669583..14693036hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3823454
hg1923454
hg1823454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564778
Samples
Known GenesZNF333
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060306
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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