A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580120



Internal ID16367529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54052839..54056824hg38UCSC Ensembl
Innerchr19:54556093..54560078hg19UCSC Ensembl
Innerchr19:59247905..59251890hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383986
hg193986
hg183986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6543n54
Supporting Variantsnssv901203, nssv901201, nssv901205, nssv901204, nssv901202, nssv901206
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580120
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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