A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580137



Internal ID16020860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54053501..54058538hg38UCSC Ensembl
Innerchr19:54556755..54561792hg19UCSC Ensembl
Innerchr19:59248567..59253604hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg385038
hg195038
hg185038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901356, nssv901355
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580137
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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