A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524823



Internal ID18476418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91050554..91072656hg38UCSC Ensembl
Innerchr12:91444331..91466433hg19UCSC Ensembl
Innerchr12:89968462..89990564hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3822103
hg1922103
hg1822103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039417
Supporting Variants
Samples
Known GenesKERA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524823
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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