A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703704



Internal ID15093670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69916038..70100576hg38UCSC Ensembl
Innerchr8:70828273..71012811hg19UCSC Ensembl
Innerchr8:70990827..71175365hg18UCSC Ensembl
Innerchr8:70990827..71175365hg17UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38184539
hg19184539
hg18184539
hg17184539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527289
Supporting Variants
Samples
Known GenesPRDM14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703704
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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