A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033049



Internal ID19122271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14039295..14109037hg38UCSC Ensembl
Innerchr8:13896804..13966546hg19UCSC Ensembl
Innerchr8:13941175..14010917hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3869743
hg1969743
hg1869743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7101n100
Supporting Variantsnssv3675856
Samples
Known GenesSGCZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033049
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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