A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998493



Internal ID19158029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690340..109707956hg38UCSC Ensembl
Innerchr1:110232962..110250578hg19UCSC Ensembl
Innerchr1:110034485..110052101hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817617
hg1917617
hg1817617
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n100
Supporting Variantsnssv3492083, nssv3485223, nssv3702404, nssv3499286, nssv3492637, nssv3702405, nssv3702403, nssv3495511, nssv3485578, nssv3499279, nssv3487338, nssv3491552, nssv3485065
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)nsv998493
Frequency
Sample Size11257
Observed Gain9
Observed Loss4
Observed Complex0
Frequencyn/a


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