A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000373



Internal ID19089590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63137507..63471975hg38UCSC Ensembl
Innerchr4:64003225..64337693hg19UCSC Ensembl
Innerchr4:63685820..64020288hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38334469
hg19334469
hg18334469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626533
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)nsv1000373
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