A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001067



Internal ID19090284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109679093..109697544hg38UCSC Ensembl
Innerchr1:110221715..110240166hg19UCSC Ensembl
Innerchr1:110023238..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818452
hg1918452
hg1818452
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n100
Supporting Variantsnssv3495601, nssv3499183, nssv3484837, nssv3502717, nssv3495979, nssv3497424, nssv3495464
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)nsv1001067
Frequency
Sample Size11257
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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