A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006728



Internal ID19095946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109677464..109697544hg38UCSC Ensembl
Innerchr1:110220086..110240166hg19UCSC Ensembl
Innerchr1:110021609..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3820081
hg1920081
hg1820081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv261n100
Supporting Variantsnssv3495110, nssv3486580, nssv3487570, nssv3500556
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)nsv1006728
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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