A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023220



Internal ID19112437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156864876..156894735hg38UCSC Ensembl
Innerchr4:157786028..157815887hg19UCSC Ensembl
Innerchr4:158005478..158035337hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3829860
hg1929860
hg1829860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636144, nssv3636145
Samples
Known GenesPDGFC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023220
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