A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024309



Internal ID19113526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:135618416..135680874hg38UCSC Ensembl
Innerchr4:136539571..136602029hg19UCSC Ensembl
Innerchr4:136759021..136821479hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3862459
hg1962459
hg1862459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5400n100
Supporting Variantsnssv3641109, nssv3641110
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)nsv1024309
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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