A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689774



Internal ID15079740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94253949..94257296hg38UCSC Ensembl
Innerchr6:94963667..94967014hg19UCSC Ensembl
Innerchr6:95020388..95023735hg18UCSC Ensembl
Innerchr6:95020388..95023735hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383348
hg193348
hg183348
hg173348
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689774
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