A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999622



Internal ID18812472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109658958..109697544hg38UCSC Ensembl
Innerchr1:110201580..110240166hg19UCSC Ensembl
Innerchr1:110003103..110041689hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3838587
hg1938587
hg1838587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv258n100
Supporting Variantsnssv3484766, nssv3497033
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)nsv999622
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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