A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019864



Internal ID19109082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12520123hg38UCSC Ensembl
Innerchr8:12260915..12377632hg19UCSC Ensembl
Innerchr8:12305286..12422003hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38116718
hg19116718
hg18116718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7069n100
Supporting Variantsnssv3665904, nssv3665902, nssv3665905, nssv3665903
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019864
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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