A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669604



Internal ID15406256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:46422027..46436193hg38UCSC Ensembl
Innerchr21:47841941..47856106hg19UCSC Ensembl
Innerchr21:46666369..46680534hg18UCSC Ensembl
Innerchr21:46666369..46680534hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3814167
hg1914166
hg1814166
hg1714166
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515801
Supporting Variants
Samples
Known GenesPCNT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669604
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