A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610199



Internal ID16397608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8892572..8893806hg38UCSC Ensembl
Innerchr8:8750082..8751316hg19UCSC Ensembl
Innerchr8:8787492..8788726hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381235
hg191235
hg181235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11942n54
Supporting Variantsnssv1105981
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610199
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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