A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011397



Internal ID18753931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109650144..109697544hg38UCSC Ensembl
Innerchr1:110192766..110240166hg19UCSC Ensembl
Innerchr1:109994289..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3847401
hg1947401
hg1847401
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv254n100
Supporting Variantsnssv3498636, nssv3496694, nssv3502346, nssv3490344, nssv3495751, nssv3701156, nssv3492557, nssv3499554
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011397
Frequency
Sample Size29084
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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