A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005106



Internal ID19094323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109679093..109700319hg38UCSC Ensembl
Innerchr1:110221715..110242941hg19UCSC Ensembl
Innerchr1:110023238..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3821227
hg1921227
hg1821227
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n100
Supporting Variantsnssv3491792, nssv3488288, nssv3496222, nssv3490078, nssv3502592, nssv3490212, nssv3494938, nssv3491567, nssv3490400, nssv3492661, nssv3500368, nssv3495092, nssv3487038, nssv3499304, nssv3499312, nssv3496880, nssv3487058, nssv3496736, nssv3486581
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)nsv1005106
Frequency
Sample Size11257
Observed Gain18
Observed Loss1
Observed Complex0
Frequencyn/a


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