A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680994



Internal ID15417646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31851236..31910068hg38UCSC Ensembl
Innerchr12:32004170..32063002hg19UCSC Ensembl
Innerchr12:31895437..31954269hg18UCSC Ensembl
Innerchr12:31895437..31954269hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3858833
hg1958833
hg1858833
hg1758833
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516507
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680994
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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