A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801990



Internal ID16095946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:109713735..109714679hg38UCSC Ensembl
Innerchr12:110151540..110152484hg19UCSC Ensembl
Innerchr12:108635923..108636867hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38945
hg19945
hg18945
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560144
Supporting Variants
Samples
Known GenesFAM222A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801990
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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