A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892209



Internal ID16186165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2841299..2842116hg38UCSC Ensembl
Innerchr19:2841297..2842114hg19UCSC Ensembl
Innerchr19:2792297..2793114hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38818
hg19818
hg18818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578414
Supporting Variants
Samples
Known GenesZNF555
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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