A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610190



Internal ID16050913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8886730..8909371hg38UCSC Ensembl
Innerchr8:8744240..8766881hg19UCSC Ensembl
Innerchr8:8781650..8804291hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3822642
hg1922642
hg1822642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105957
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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