A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664114



Internal ID15054080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168031556..168096766hg38UCSC Ensembl
Innerchr6:168432236..168497446hg19UCSC Ensembl
Innerchr6:168175085..168240295hg18UCSC Ensembl
Innerchr6:168250792..168316002hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3865211
hg1965211
hg1865211
hg1765211
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515568
Supporting Variants
Samples
Known GenesFRMD1, KIF25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664114
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