A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009333



Internal ID18751864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126006809..126041785hg38UCSC Ensembl
Innerchr3:125725652..125760628hg19UCSC Ensembl
Innerchr3:127208342..127243318hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3834977
hg1934977
hg1834977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603493
Samples
Known GenesSLC41A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009333
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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