A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3496952



Internal ID18737907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683506..109710508hg38UCSC Ensembl
Innerchr1:110226128..110253130hg19UCSC Ensembl
Innerchr1:110027651..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3827003
hg1927003
hg1827003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010300
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)nssv3496952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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