A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010368



Internal ID18752899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683506..109707602hg38UCSC Ensembl
Innerchr1:110226128..110250224hg19UCSC Ensembl
Innerchr1:110027651..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3824097
hg1924097
hg1824097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv273n100
Supporting Variantsnssv3493212
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)nsv1010368
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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