A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656259



Internal ID15046225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52043707..52045965hg38UCSC Ensembl
Innerchr12:52437491..52439749hg19UCSC Ensembl
Innerchr12:50723758..50726016hg18UCSC Ensembl
Innerchr12:50723758..50726016hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg382259
hg192259
hg182259
hg172259
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518451
Supporting Variants
Samples
Known GenesNR4A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656259
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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