A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv795909



Internal ID16089865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:51816307..51821428hg38UCSC Ensembl
Innerchr12:52210091..52215212hg19UCSC Ensembl
Innerchr12:50496358..50501479hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg385122
hg195122
hg185122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558878
Supporting Variants
Samples
Known GenesFIGNL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv795909
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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