A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662267



Internal ID15052233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:126285387..126415470hg38UCSC Ensembl
Innerchr12:126769933..126900016hg19UCSC Ensembl
Innerchr12:125335886..125465969hg18UCSC Ensembl
Innerchr12:125294813..125424896hg17UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38130084
hg19130084
hg18130084
hg17130084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515762
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662267
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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