A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689662



Internal ID15079628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94148171..94179870hg38UCSC Ensembl
Innerchr11:93881337..93913036hg19UCSC Ensembl
Innerchr11:93520985..93552684hg18UCSC Ensembl
Innerchr11:93520985..93552684hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3831700
hg1931700
hg1831700
hg1731700
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517664
Supporting Variants
Samples
Known GenesPANX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689662
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