A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030987



Internal ID19120208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167389364..167555226hg38UCSC Ensembl
Innerchr4:168310515..168476377hg19UCSC Ensembl
Innerchr4:168547090..168712952hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38165863
hg19165863
hg18165863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634177
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)nsv1030987
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