A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699224



Internal ID15089190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65329708..65342782hg38UCSC Ensembl
Innerchr6:66039601..66052675hg19UCSC Ensembl
Innerchr6:66096322..66109396hg18UCSC Ensembl
Innerchr6:66096322..66109396hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3813075
hg1913075
hg1813075
hg1713075
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516417
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699224
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