A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760197



Internal ID19058478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13003628..13071858hg38UCSC Ensembl
Innerchr8:12861137..12929367hg19UCSC Ensembl
Innerchr8:12905508..12973738hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3868231
hg1968231
hg1868231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026381
Supporting Variants
Samples
Known GenesKIAA1456
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760197
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