A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004586



Internal ID19093803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16340250..16373541hg38UCSC Ensembl
Innerchr4:16341873..16375164hg19UCSC Ensembl
Innerchr4:15950971..15984262hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3833292
hg1933292
hg1833292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5147n100
Supporting Variantsnssv3619865, nssv3619866
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)nsv1004586
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