A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578426



Internal ID16019149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:3937221..3938141hg38UCSC Ensembl
Innerchr19:3937219..3938139hg19UCSC Ensembl
Innerchr19:3888219..3889139hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38921
hg19921
hg18921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6228n54
Supporting Variantsnssv892836, nssv892837, nssv892835
Samples
Known GenesNMRK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578426
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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