A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789874



Internal ID15737144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:26945269..26966684hg38UCSC Ensembl
Innerchr12:27098202..27119617hg19UCSC Ensembl
Innerchr12:26989469..27010884hg18UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg3821416
hg1921416
hg1821416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557804
Supporting Variants
Samples
Known GenesFGFR1OP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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