A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3498964



Internal ID18739919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690403..109707956hg38UCSC Ensembl
Innerchr1:110233025..110250578hg19UCSC Ensembl
Innerchr1:110034548..110052101hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817554
hg1917554
hg1817554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998361
Supporting Variants
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3498964
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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