A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580144



Internal ID16367553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54054016..54057172hg38UCSC Ensembl
Innerchr19:54557270..54560426hg19UCSC Ensembl
Innerchr19:59249082..59252238hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383157
hg193157
hg183157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6543n54
Supporting Variantsnssv901380, nssv901386, nssv901381, nssv901383, nssv901384, nssv901379, nssv901387, nssv901388, nssv901385, nssv901382
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580144
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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