A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681867



Internal ID15071833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:126285387..126413600hg38UCSC Ensembl
Innerchr12:126769933..126898146hg19UCSC Ensembl
Innerchr12:125335886..125464099hg18UCSC Ensembl
Innerchr12:125294813..125423026hg17UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38128214
hg19128214
hg18128214
hg17128214
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)nssv681867
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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