A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643178



Internal ID18941459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15297206..15515787hg38UCSC Ensembl
Innerchr7:15336831..15555412hg19UCSC Ensembl
Innerchr7:15303356..15521937hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38218582
hg19218582
hg18218582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028314
Supporting Variants
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643178
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