A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493366



Internal ID18734321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681750..109703496hg38UCSC Ensembl
Innerchr1:110224372..110246118hg19UCSC Ensembl
Innerchr1:110025895..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3821747
hg1921747
hg1821747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004507
Supporting Variants
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493366
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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