A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578206



Internal ID16018929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049570..1049882hg38UCSC Ensembl
Innerchr19:1049569..1049881hg19UCSC Ensembl
Innerchr19:1000569..1000881hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38313
hg19313
hg18313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6183n54
Supporting Variantsnssv891508, nssv891509, nssv891511, nssv891510
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578206
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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