A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578068



Internal ID16365477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:404077..497458hg38UCSC Ensembl
Innerchr19:404077..497458hg19UCSC Ensembl
Innerchr19:355077..448458hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3893382
hg1993382
hg1893382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6155n54
Supporting Variantsnssv890946, nssv890944, nssv890943, nssv890945
Samples
Known GenesC2CD4C, MADCAM1, ODF3L2, SHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578068
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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