A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760121



Internal ID19058402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12486092hg38UCSC Ensembl
Innerchr8:12260915..12343601hg19UCSC Ensembl
Innerchr8:12305286..12387972hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3882687
hg1982687
hg1882687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020711
Supporting Variants
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)nssv3760121
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