A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3681713



Internal ID18979994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10090832..10156645hg38UCSC Ensembl
Innerchr8:9948342..10014155hg19UCSC Ensembl
Innerchr8:9985752..10051565hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3865814
hg1965814
hg1865814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034343
Supporting Variants
Samples
Known GenesMSRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3681713
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