A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005433



Internal ID18747964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684762..109707602hg38UCSC Ensembl
Innerchr1:110227384..110250224hg19UCSC Ensembl
Innerchr1:110028907..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3822841
hg1922841
hg1822841
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv272n100
Supporting Variantsnssv3497445, nssv3499968, nssv3484349, nssv3702359
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)nsv1005433
Frequency
Sample Size29084
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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