A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023774



Internal ID18766307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157782180..157852922hg38UCSC Ensembl
Innerchr5:157209188..157279930hg19UCSC Ensembl
Innerchr5:157141766..157212508hg18UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3870743
hg1970743
hg1870743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648220
Samples
Known GenesCLINT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023774
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer