A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685350



Internal ID18636945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21915873..21970322hg38UCSC Ensembl
Innerchr8:21773384..21827833hg19UCSC Ensembl
Innerchr8:21829330..21883779hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3854450
hg1954450
hg1854450
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034809
Supporting Variants
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685350
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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