A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580357



Internal ID16367766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56339580..56358425hg38UCSC Ensembl
Innerchr19:56850949..56869794hg19UCSC Ensembl
Innerchr19:61542761..61561606hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3818846
hg1918846
hg1818846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6584n54
Supporting Variantsnssv901823
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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