A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516652



Internal ID15443945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152764162..152811207hg38UCSC Ensembl
Innerchr4:153685314..153732359hg19UCSC Ensembl
Innerchr4:153904764..153951809hg18UCSC Ensembl
Innerchr4:154042919..154089964hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3847046
hg1947046
hg1847046
hg1747046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653286, nssv692734, nssv687223, nssv668183, nssv689185, nssv658998, nssv691631, nssv666463, nssv665936, nssv672711, nssv655612, nssv668231, nssv684682, nssv654814, nssv656169, nssv657481, nssv667850, nssv677622, nssv684137, nssv656982, nssv687592, nssv661722, nssv671814, nssv693017
Samples
Known GenesARFIP1, TIGD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516652
Frequency
Sample Size2026
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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