A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579856



Internal ID16020579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44351605..44395657hg38UCSC Ensembl
Innerchr19:44855757..44899820hg19UCSC Ensembl
Innerchr19:49547597..49591660hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3844053
hg1944064
hg1844064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899920
Samples
Known GenesZNF112, ZNF285
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579856
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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