A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578196



Internal ID16018919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049519..1049621hg38UCSC Ensembl
Innerchr19:1049518..1049620hg19UCSC Ensembl
Innerchr19:1000518..1000620hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891357, nssv891358
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578196
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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