A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3488961



Internal ID18729916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683286..109700319hg38UCSC Ensembl
Innerchr1:110225908..110242941hg19UCSC Ensembl
Innerchr1:110027431..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817034
hg1917034
hg1817034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015095
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)nssv3488961
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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