A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703480



Internal ID15440132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7927803..7931373hg38UCSC Ensembl
Innerchr11:7949350..7952920hg19UCSC Ensembl
Innerchr11:7905926..7909496hg18UCSC Ensembl
Innerchr11:7905926..7909496hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383571
hg193571
hg183571
hg173571
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527100
Supporting Variants
Samples
Known GenesOR10A6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703480
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