A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578536



Internal ID16365945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7870830..7871660hg38UCSC Ensembl
Innerchr19:7935716..7936546hg19UCSC Ensembl
Innerchr19:7841716..7842546hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38831
hg19831
hg18831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893301
Samples
Known GenesFLJ22184
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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