A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643141



Internal ID18941422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13639878..13694022hg38UCSC Ensembl
Innerchr7:13679503..13733647hg19UCSC Ensembl
Innerchr7:13646028..13700172hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3854145
hg1954145
hg1854145
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029362
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643141
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