A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579878



Internal ID16020601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119519..46124876hg38UCSC Ensembl
Innerchr19:46622776..46628133hg19UCSC Ensembl
Innerchr19:51314616..51319973hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385358
hg195358
hg185358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6504n54
Supporting Variantsnssv899948, nssv899950, nssv899951, nssv899949
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579878
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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