A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005620



Internal ID18748151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62112397..62169669hg38UCSC Ensembl
Innerchr4:62978115..63035387hg19UCSC Ensembl
Innerchr4:62660710..62717982hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3857273
hg1957273
hg1857273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739496
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005620
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