A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703392



Internal ID15093358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14104569..14110284hg38UCSC Ensembl
Innerchr21:15476890..15482605hg19UCSC Ensembl
Innerchr21:14398761..14404476hg18UCSC Ensembl
Innerchr21:14398761..14404476hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg385716
hg195716
hg185716
hg175716
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527017
Supporting Variants
Samples
Known GenesLIPI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703392
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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