A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706021



Internal ID15442673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59546924..59548794hg38UCSC Ensembl
Innerchr18:57214156..57216026hg19UCSC Ensembl
Innerchr18:55365136..55367006hg18UCSC Ensembl
Innerchr18:55365136..55367006hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg381871
hg191871
hg181871
hg171871
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522624
Supporting Variants
Samples
Known GenesCCBE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706021
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