A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524602



Internal ID18822883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:67531238..67569459hg38UCSC Ensembl
Innerchr12:67925018..67963239hg19UCSC Ensembl
Innerchr12:66211285..66249506hg18UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3838222
hg1938222
hg1838222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040339
Supporting Variants
Samples
Known GenesLOC100507175
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3524602
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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