A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010142



Internal ID19099361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681750..109691994hg38UCSC Ensembl
Innerchr1:110224372..110234616hg19UCSC Ensembl
Innerchr1:110025895..110036139hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3810245
hg1910245
hg1810245
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n100
Supporting Variantsnssv3492818, nssv3487271, nssv3486602, nssv3495598
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)nsv1010142
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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