A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491704



Internal ID19079345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690340..109708523hg38UCSC Ensembl
Innerchr1:110232962..110251145hg19UCSC Ensembl
Innerchr1:110034485..110052668hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818184
hg1918184
hg1818184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003898
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)nssv3491704
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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