A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972392



Internal ID15919662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126014238..126076708hg38UCSC Ensembl
Innerchr3:125733081..125795551hg19UCSC Ensembl
Innerchr3:127215771..127278241hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3862471
hg1962471
hg1862471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591492
Supporting Variants
Samples
Known GenesSLC41A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972392
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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