A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610202



Internal ID16050925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8892675..8893832hg38UCSC Ensembl
Innerchr8:8750185..8751342hg19UCSC Ensembl
Innerchr8:8787595..8788752hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381158
hg191158
hg181158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11943n54
Supporting Variantsnssv1105985
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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