A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023201



Internal ID19112418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12418220..12520766hg38UCSC Ensembl
Innerchr8:12275729..12378275hg19UCSC Ensembl
Innerchr8:12320100..12422646hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38102547
hg19102547
hg18102547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7069n100
Supporting Variantsnssv3666909
Samples
Known GenesFAM86B2, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023201
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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