A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892827



Internal ID16186783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3804703..3835179hg38UCSC Ensembl
Innerchr19:3804701..3835177hg19UCSC Ensembl
Innerchr19:3755701..3786177hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3830477
hg1930477
hg1830477
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578421
Supporting Variants
Samples
Known GenesZFR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892827
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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