A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3483882



Internal ID18724837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683506..109703496hg38UCSC Ensembl
Innerchr1:110226128..110246118hg19UCSC Ensembl
Innerchr1:110027651..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819991
hg1919991
hg1819991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997730
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)nssv3483882
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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