A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578798



Internal ID16019521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19752205..19838400hg38UCSC Ensembl
Innerchr19:19863014..19949209hg19UCSC Ensembl
Innerchr19:19724014..19810209hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3886196
hg1986196
hg1886196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149849
SamplesHGDP00776
Known GenesLINC00663, ZNF506
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578798
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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