A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578203



Internal ID16018926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1049570..1049675hg38UCSC Ensembl
Innerchr19:1049569..1049674hg19UCSC Ensembl
Innerchr19:1000569..1000674hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38106
hg19106
hg18106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891430, nssv891429, nssv891428
Samples
Known GenesABCA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578203
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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