A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013002



Internal ID18755533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684762..109710508hg38UCSC Ensembl
Innerchr1:110227384..110253130hg19UCSC Ensembl
Innerchr1:110028907..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3825747
hg1925747
hg1825747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv273n100
Supporting Variantsnssv3499515, nssv3702362, nssv3489021, nssv3494916
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)nsv1013002
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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