A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892071



Internal ID15839341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2214058..2285197hg38UCSC Ensembl
Innerchr19:2214057..2285196hg19UCSC Ensembl
Innerchr19:2165057..2236196hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3871140
hg1971140
hg1871140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578383
Supporting Variants
Samples
Known GenesAMH, C19orf35, DOT1L, JSRP1, MIR1227, MIR4321, MIR6789, OAZ1, PLEKHJ1, SF3A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892071
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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