A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031070



Internal ID19120291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167073427..167133881hg38UCSC Ensembl
Innerchr4:167994578..168055032hg19UCSC Ensembl
Innerchr4:168231153..168291607hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3860455
hg1960455
hg1860455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744490
Samples
Known GenesSPOCK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031070
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