A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643031



Internal ID18941312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13054314..13091020hg38UCSC Ensembl
Innerchr7:13093939..13130645hg19UCSC Ensembl
Innerchr7:13060464..13097170hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836707
hg1936707
hg1836707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016921
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)nssv3643031
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