A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016190



Internal ID19105409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12423600..12624526hg38UCSC Ensembl
Innerchr8:12281109..12482035hg19UCSC Ensembl
Innerchr8:12325480..12526406hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38200927
hg19200927
hg18200927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7064n100
Supporting Variantsnssv3666915
Samples
Known GenesFAM86B2, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016190
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer