A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521913



Internal ID18820194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:45001..106873hg38UCSC Ensembl
Innerchr12:150430..216039hg19UCSC Ensembl
Innerchr12:20691..86300hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3861873
hg1965610
hg1865610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054172
Supporting Variants
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521913
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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