A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176297



Internal ID15880046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31851236..31915943hg38UCSC Ensembl
Innerchr12:32004170..32068877hg19UCSC Ensembl
Innerchr12:31895437..31960144hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3864708
hg1964708
hg1864708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558148
Supporting Variants
SamplesNINDS_146
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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