A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689421



Internal ID15079387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73057625..73059727hg38UCSC Ensembl
Innerchr17:71053764..71055866hg19UCSC Ensembl
Innerchr17:68565359..68567461hg18UCSC Ensembl
Innerchr17:68565359..68567461hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
hg172103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519473
Supporting Variants
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689421
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