A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578626



Internal ID16366035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12491203..12498204hg38UCSC Ensembl
Innerchr19:12602017..12609018hg19UCSC Ensembl
Innerchr19:12463017..12470018hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387002
hg197002
hg187002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893564
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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