A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024430



Internal ID19113647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176030941..176128676hg38UCSC Ensembl
Innerchr4:176952092..177049827hg19UCSC Ensembl
Innerchr4:177189086..177286821hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3897736
hg1997736
hg1897736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635456
Samples
Known GenesMIR1267, WDR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024430
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