A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028153



Internal ID19117371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139100120..139122287hg38UCSC Ensembl
Innerchr4:140021274..140043441hg19UCSC Ensembl
Innerchr4:140240724..140262891hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3822168
hg1922168
hg1822168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641182
Samples
Known GenesELF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028153
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