A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698093



Internal ID15088059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9000550..9001336hg38UCSC Ensembl
Innerchr12:9153146..9153932hg19UCSC Ensembl
Innerchr12:9044413..9045199hg18UCSC Ensembl
Innerchr12:9044413..9045199hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
hg17787
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521482
Supporting Variants
Samples
Known GenesKLRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698093
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