A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999677



Internal ID19159213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109681750..109694313hg38UCSC Ensembl
Innerchr1:110224372..110236935hg19UCSC Ensembl
Innerchr1:110025895..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3812564
hg1912564
hg1812564
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n100
Supporting Variantsnssv3498843, nssv3490756, nssv3701183, nssv3497992, nssv3701184
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)nsv999677
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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