A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478359



Internal ID19068050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8059202..8315853hg38UCSC Ensembl
Innerchr1:8119262..8375913hg19UCSC Ensembl
Innerchr1:8041849..8298500hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38256652
hg19256652
hg18256652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014727
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)nssv3478359
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