A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892836



Internal ID15840106
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 StatusS
Merged Variantsnsv578426
Supporting Variants
Samples
Known GenesNMRK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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