A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025612



Internal ID19114830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12382797..12486092hg38UCSC Ensembl
Innerchr8:12240306..12343601hg19UCSC Ensembl
Innerchr8:12284677..12387972hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38103296
hg19103296
hg18103296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7058n100
Supporting Variantsnssv3664851
Samples
Known GenesDEFB109P1, FAM66A, 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)nsv1025612
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