A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017900



Internal ID19107117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45935900..46112758hg38UCSC Ensembl
Innerchr8:46847522..47024380hg19UCSC Ensembl
Innerchr8:46966687..47143545hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38176859
hg19176859
hg18176859
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7200n100
Supporting Variantsnssv3687370, nssv3687371
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)nsv1017900
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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