A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026272



Internal ID19115489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178405237..178777205hg38UCSC Ensembl
Innerchr4:179326391..179698359hg19UCSC Ensembl
Innerchr4:179563385..179935353hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38371969
hg19371969
hg18371969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635554
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)nsv1026272
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