A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891811



Internal ID16185767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1566455..1567339hg38UCSC Ensembl
Innerchr19:1566454..1567338hg19UCSC Ensembl
Innerchr19:1517454..1518338hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38885
hg19885
hg18885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578300
Supporting Variants
Samples
Known GenesMEX3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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