A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023221



Internal ID19112438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8837883..8864908hg38UCSC Ensembl
Innerchr8:8695393..8722418hg19UCSC Ensembl
Innerchr8:8732803..8759828hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827026
hg1927026
hg1827026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3681691
Samples
Known GenesMFHAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023221
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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